Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Guinovart, R.M. [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2014transfer abstract |
|---|
| Schlagwörter: |
|---|
| Umfang: |
6 |
|---|
| Übergeordnetes Werk: |
Enthalten in: Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? - Madias, John E. ELSEVIER, 2014, Barcelona [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:105 ; year:2014 ; number:2 ; pages:1-6 ; extent:6 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.adengl.2013.03.012 |
|---|
| Katalog-ID: |
ELV033785015 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | ELV033785015 | ||
| 003 | DE-627 | ||
| 005 | 20230625195016.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 180603s2014 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1016/j.adengl.2013.03.012 |2 doi | |
| 028 | 5 | 2 | |a GBVA2014007000011.pica |
| 035 | |a (DE-627)ELV033785015 | ||
| 035 | |a (ELSEVIER)S1578-2190(14)00025-0 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | |a 610 | |
| 082 | 0 | 4 | |a 610 |q DE-600 |
| 082 | 0 | 4 | |a 610 |q VZ |
| 082 | 0 | 4 | |a 630 |a 640 |a 610 |q VZ |
| 100 | 1 | |a Guinovart, R.M. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases |
| 264 | 1 | |c 2014transfer abstract | |
| 300 | |a 6 | ||
| 336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
| 337 | |a nicht spezifiziert |b z |2 rdamedia | ||
| 338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
| 520 | |a Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. | ||
| 520 | |a Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. | ||
| 650 | 7 | |a Clonality |2 Elsevier | |
| 650 | 7 | |a Angiolymphoid hyperplasia with eosinophilia |2 Elsevier | |
| 650 | 7 | |a Kimura disease |2 Elsevier | |
| 700 | 1 | |a Bassas-Vila, J. |4 oth | |
| 700 | 1 | |a Morell, L. |4 oth | |
| 700 | 1 | |a Ferrándiz, C. |4 oth | |
| 773 | 0 | 8 | |i Enthalten in |n Elsevier España |a Madias, John E. ELSEVIER |t Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? |d 2014 |g Barcelona [u.a.] |w (DE-627)ELV012118117 |
| 773 | 1 | 8 | |g volume:105 |g year:2014 |g number:2 |g pages:1-6 |g extent:6 |
| 856 | 4 | 0 | |u https://doi.org/10.1016/j.adengl.2013.03.012 |3 Volltext |
| 912 | |a GBV_USEFLAG_U | ||
| 912 | |a GBV_ELV | ||
| 912 | |a SYSFLAG_U | ||
| 912 | |a SSG-OLC-PHA | ||
| 912 | |a GBV_ILN_24 | ||
| 951 | |a AR | ||
| 952 | |d 105 |j 2014 |e 2 |h 1-6 |g 6 |y 105.2014, 2, e1-, (6 S.) | ||
| 953 | |2 045F |a 610 | ||
| author_variant |
r g rg |
|---|---|
| matchkey_str |
guinovartrmbassasvilajmorelllferrndizc:2014----:nilmhihprlsaihoiohlaciioa |
| hierarchy_sort_str |
2014transfer abstract |
| publishDate |
2014 |
| allfields |
10.1016/j.adengl.2013.03.012 doi GBVA2014007000011.pica (DE-627)ELV033785015 (ELSEVIER)S1578-2190(14)00025-0 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 630 640 610 VZ Guinovart, R.M. verfasserin aut Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases 2014transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Elsevier Bassas-Vila, J. oth Morell, L. oth Ferrándiz, C. oth Enthalten in Elsevier España Madias, John E. ELSEVIER Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? 2014 Barcelona [u.a.] (DE-627)ELV012118117 volume:105 year:2014 number:2 pages:1-6 extent:6 https://doi.org/10.1016/j.adengl.2013.03.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 AR 105 2014 2 1-6 6 105.2014, 2, e1-, (6 S.) 045F 610 |
| spelling |
10.1016/j.adengl.2013.03.012 doi GBVA2014007000011.pica (DE-627)ELV033785015 (ELSEVIER)S1578-2190(14)00025-0 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 630 640 610 VZ Guinovart, R.M. verfasserin aut Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases 2014transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Elsevier Bassas-Vila, J. oth Morell, L. oth Ferrándiz, C. oth Enthalten in Elsevier España Madias, John E. ELSEVIER Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? 2014 Barcelona [u.a.] (DE-627)ELV012118117 volume:105 year:2014 number:2 pages:1-6 extent:6 https://doi.org/10.1016/j.adengl.2013.03.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 AR 105 2014 2 1-6 6 105.2014, 2, e1-, (6 S.) 045F 610 |
| allfields_unstemmed |
10.1016/j.adengl.2013.03.012 doi GBVA2014007000011.pica (DE-627)ELV033785015 (ELSEVIER)S1578-2190(14)00025-0 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 630 640 610 VZ Guinovart, R.M. verfasserin aut Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases 2014transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Elsevier Bassas-Vila, J. oth Morell, L. oth Ferrándiz, C. oth Enthalten in Elsevier España Madias, John E. ELSEVIER Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? 2014 Barcelona [u.a.] (DE-627)ELV012118117 volume:105 year:2014 number:2 pages:1-6 extent:6 https://doi.org/10.1016/j.adengl.2013.03.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 AR 105 2014 2 1-6 6 105.2014, 2, e1-, (6 S.) 045F 610 |
| allfieldsGer |
10.1016/j.adengl.2013.03.012 doi GBVA2014007000011.pica (DE-627)ELV033785015 (ELSEVIER)S1578-2190(14)00025-0 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 630 640 610 VZ Guinovart, R.M. verfasserin aut Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases 2014transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Elsevier Bassas-Vila, J. oth Morell, L. oth Ferrándiz, C. oth Enthalten in Elsevier España Madias, John E. ELSEVIER Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? 2014 Barcelona [u.a.] (DE-627)ELV012118117 volume:105 year:2014 number:2 pages:1-6 extent:6 https://doi.org/10.1016/j.adengl.2013.03.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 AR 105 2014 2 1-6 6 105.2014, 2, e1-, (6 S.) 045F 610 |
| allfieldsSound |
10.1016/j.adengl.2013.03.012 doi GBVA2014007000011.pica (DE-627)ELV033785015 (ELSEVIER)S1578-2190(14)00025-0 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 630 640 610 VZ Guinovart, R.M. verfasserin aut Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases 2014transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Elsevier Bassas-Vila, J. oth Morell, L. oth Ferrándiz, C. oth Enthalten in Elsevier España Madias, John E. ELSEVIER Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? 2014 Barcelona [u.a.] (DE-627)ELV012118117 volume:105 year:2014 number:2 pages:1-6 extent:6 https://doi.org/10.1016/j.adengl.2013.03.012 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 AR 105 2014 2 1-6 6 105.2014, 2, e1-, (6 S.) 045F 610 |
| language |
English |
| source |
Enthalten in Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? Barcelona [u.a.] volume:105 year:2014 number:2 pages:1-6 extent:6 |
| sourceStr |
Enthalten in Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? Barcelona [u.a.] volume:105 year:2014 number:2 pages:1-6 extent:6 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| topic_facet |
Clonality Angiolymphoid hyperplasia with eosinophilia Kimura disease |
| dewey-raw |
610 |
| isfreeaccess_bool |
false |
| container_title |
Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? |
| authorswithroles_txt_mv |
Guinovart, R.M. @@aut@@ Bassas-Vila, J. @@oth@@ Morell, L. @@oth@@ Ferrándiz, C. @@oth@@ |
| publishDateDaySort_date |
2014-01-01T00:00:00Z |
| hierarchy_top_id |
ELV012118117 |
| dewey-sort |
3610 |
| id |
ELV033785015 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV033785015</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625195016.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2014 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.adengl.2013.03.012</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2014007000011.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV033785015</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S1578-2190(14)00025-0</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">630</subfield><subfield code="a">640</subfield><subfield code="a">610</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Guinovart, R.M.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2014transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">6</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Clonality</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Angiolymphoid hyperplasia with eosinophilia</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Kimura disease</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bassas-Vila, J.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Morell, L.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ferrándiz, C.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier España</subfield><subfield code="a">Madias, John E. ELSEVIER</subfield><subfield code="t">Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome?</subfield><subfield code="d">2014</subfield><subfield code="g">Barcelona [u.a.]</subfield><subfield code="w">(DE-627)ELV012118117</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:105</subfield><subfield code="g">year:2014</subfield><subfield code="g">number:2</subfield><subfield code="g">pages:1-6</subfield><subfield code="g">extent:6</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.adengl.2013.03.012</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">105</subfield><subfield code="j">2014</subfield><subfield code="e">2</subfield><subfield code="h">1-6</subfield><subfield code="g">6</subfield><subfield code="y">105.2014, 2, e1-, (6 S.)</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">610</subfield></datafield></record></collection>
|
| author |
Guinovart, R.M. |
| spellingShingle |
Guinovart, R.M. ddc 610 ddc 630 Elsevier Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases |
| authorStr |
Guinovart, R.M. |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)ELV012118117 |
| format |
electronic Article |
| dewey-ones |
610 - Medicine & health 630 - Agriculture & related technologies 640 - Home & family management |
| delete_txt_mv |
keep |
| author_role |
aut |
| collection |
elsevier |
| remote_str |
true |
| illustrated |
Not Illustrated |
| topic_title |
610 610 DE-600 610 VZ 630 640 610 VZ Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease Elsevier |
| topic |
ddc 610 ddc 630 Elsevier Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease |
| topic_unstemmed |
ddc 610 ddc 630 Elsevier Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease |
| topic_browse |
ddc 610 ddc 630 Elsevier Clonality Elsevier Angiolymphoid hyperplasia with eosinophilia Elsevier Kimura disease |
| format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
zu |
| author2_variant |
j b v jbv l m lm c f cf |
| hierarchy_parent_title |
Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? |
| hierarchy_parent_id |
ELV012118117 |
| dewey-tens |
610 - Medicine & health 630 - Agriculture 640 - Home & family management |
| hierarchy_top_title |
Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)ELV012118117 |
| title |
Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases |
| ctrlnum |
(DE-627)ELV033785015 (ELSEVIER)S1578-2190(14)00025-0 |
| title_full |
Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases |
| author_sort |
Guinovart, R.M. |
| journal |
Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? |
| journalStr |
Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome? |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
600 - Technology |
| recordtype |
marc |
| publishDateSort |
2014 |
| contenttype_str_mv |
zzz |
| container_start_page |
1 |
| author_browse |
Guinovart, R.M. |
| container_volume |
105 |
| physical |
6 |
| class |
610 610 DE-600 610 VZ 630 640 610 VZ |
| format_se |
Elektronische Aufsätze |
| author-letter |
Guinovart, R.M. |
| doi_str_mv |
10.1016/j.adengl.2013.03.012 |
| dewey-full |
610 630 640 |
| title_sort |
angiolymphoid hyperplasia with eosinophilia: a clinicopathologic study of 9 cases |
| title_auth |
Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases |
| abstract |
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. |
| abstractGer |
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. |
| abstract_unstemmed |
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common. |
| collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 |
| container_issue |
2 |
| title_short |
Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases |
| url |
https://doi.org/10.1016/j.adengl.2013.03.012 |
| remote_bool |
true |
| author2 |
Bassas-Vila, J. Morell, L. Ferrándiz, C. |
| author2Str |
Bassas-Vila, J. Morell, L. Ferrándiz, C. |
| ppnlink |
ELV012118117 |
| mediatype_str_mv |
z |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| author2_role |
oth oth oth |
| doi_str |
10.1016/j.adengl.2013.03.012 |
| up_date |
2024-07-06T19:27:46.371Z |
| _version_ |
1803859070940086272 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV033785015</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625195016.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2014 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.adengl.2013.03.012</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2014007000011.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV033785015</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S1578-2190(14)00025-0</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">630</subfield><subfield code="a">640</subfield><subfield code="a">610</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Guinovart, R.M.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Angiolymphoid Hyperplasia With Eosinophilia: A Clinicopathologic Study of 9 Cases</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2014transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">6</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease characterized by single or multiple angiomatous lesions typically located on the scalp and the face. We present a retrospective analysis of 9 cases of ALHE. The lesions appeared largely as multiple grouped papules or, in some cases, subcutaneous nodules, located mainly on the scalp, particularly around the ear. We also observed lesions in atypical locations, such as areas of the head other than the scalp, and the shoulder, neck, and forearm. At these sites the lesions had an atypical clinical appearance that made diagnosis difficult; this should be borne in mind in patients with single, well-delimited lesions with a vascular appearance and superficial ulceration or crusting. Surgery was the most common treatment in our series, and even though ALHE is considered a benign condition, recurrence was common.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Clonality</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Angiolymphoid hyperplasia with eosinophilia</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Kimura disease</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Bassas-Vila, J.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Morell, L.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ferrándiz, C.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier España</subfield><subfield code="a">Madias, John E. ELSEVIER</subfield><subfield code="t">Reserpine, mecamilamine, guanethidine, atropine for patients with Takotsubo syndrome?</subfield><subfield code="d">2014</subfield><subfield code="g">Barcelona [u.a.]</subfield><subfield code="w">(DE-627)ELV012118117</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:105</subfield><subfield code="g">year:2014</subfield><subfield code="g">number:2</subfield><subfield code="g">pages:1-6</subfield><subfield code="g">extent:6</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.adengl.2013.03.012</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">105</subfield><subfield code="j">2014</subfield><subfield code="e">2</subfield><subfield code="h">1-6</subfield><subfield code="g">6</subfield><subfield code="y">105.2014, 2, e1-, (6 S.)</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">610</subfield></datafield></record></collection>
|
| score |
7.400034 |