Mycosis fungoides bullosa: a case report and review of the literature

Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We pres...
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Autor*in:	Kneitz, Hermann [verfasserIn] Bröcker, Eva-B Becker, Jürgen C

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2010

Schlagwörter:	Lichen Planus Electron Beam Irradiation Mycosis Fungoides Bullous Pemphigoid Atypical Lymphocyte

Anmerkung:	© Kneitz et al; licensee BioMed Central Ltd. 2010

Übergeordnetes Werk:	Enthalten in: Journal of medical case reports - London : BioMed Central, 2007, 4(2010), 1 vom: 03. März
Übergeordnetes Werk:	volume:4 ; year:2010 ; number:1 ; day:03 ; month:03

Links:	Volltext

DOI / URN:	10.1186/1752-1947-4-78

Katalog-ID:	SPR03103408X

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520			\|a Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma.
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allfields_unstemmed	10.1186/1752-1947-4-78 doi (DE-627)SPR03103408X (SPR)1752-1947-4-78-e DE-627 ger DE-627 rakwb eng Kneitz, Hermann verfasserin aut Mycosis fungoides bullosa: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Kneitz et al; licensee BioMed Central Ltd. 2010 Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma. Lichen Planus (dpeaa)DE-He213 Electron Beam Irradiation (dpeaa)DE-He213 Mycosis Fungoides (dpeaa)DE-He213 Bullous Pemphigoid (dpeaa)DE-He213 Atypical Lymphocyte (dpeaa)DE-He213 Bröcker, Eva-B aut Becker, Jürgen C aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 03. März (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:03 month:03 https://dx.doi.org/10.1186/1752-1947-4-78 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 03 03
allfieldsGer	10.1186/1752-1947-4-78 doi (DE-627)SPR03103408X (SPR)1752-1947-4-78-e DE-627 ger DE-627 rakwb eng Kneitz, Hermann verfasserin aut Mycosis fungoides bullosa: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Kneitz et al; licensee BioMed Central Ltd. 2010 Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma. Lichen Planus (dpeaa)DE-He213 Electron Beam Irradiation (dpeaa)DE-He213 Mycosis Fungoides (dpeaa)DE-He213 Bullous Pemphigoid (dpeaa)DE-He213 Atypical Lymphocyte (dpeaa)DE-He213 Bröcker, Eva-B aut Becker, Jürgen C aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 03. März (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:03 month:03 https://dx.doi.org/10.1186/1752-1947-4-78 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 03 03
allfieldsSound	10.1186/1752-1947-4-78 doi (DE-627)SPR03103408X (SPR)1752-1947-4-78-e DE-627 ger DE-627 rakwb eng Kneitz, Hermann verfasserin aut Mycosis fungoides bullosa: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Kneitz et al; licensee BioMed Central Ltd. 2010 Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma. Lichen Planus (dpeaa)DE-He213 Electron Beam Irradiation (dpeaa)DE-He213 Mycosis Fungoides (dpeaa)DE-He213 Bullous Pemphigoid (dpeaa)DE-He213 Atypical Lymphocyte (dpeaa)DE-He213 Bröcker, Eva-B aut Becker, Jürgen C aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 03. März (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:03 month:03 https://dx.doi.org/10.1186/1752-1947-4-78 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 03 03
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topic_facet	Lichen Planus Electron Beam Irradiation Mycosis Fungoides Bullous Pemphigoid Atypical Lymphocyte
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spellingShingle	Kneitz, Hermann misc Lichen Planus misc Electron Beam Irradiation misc Mycosis Fungoides misc Bullous Pemphigoid misc Atypical Lymphocyte Mycosis fungoides bullosa: a case report and review of the literature
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topic_title	Mycosis fungoides bullosa: a case report and review of the literature Lichen Planus (dpeaa)DE-He213 Electron Beam Irradiation (dpeaa)DE-He213 Mycosis Fungoides (dpeaa)DE-He213 Bullous Pemphigoid (dpeaa)DE-He213 Atypical Lymphocyte (dpeaa)DE-He213
topic	misc Lichen Planus misc Electron Beam Irradiation misc Mycosis Fungoides misc Bullous Pemphigoid misc Atypical Lymphocyte
topic_unstemmed	misc Lichen Planus misc Electron Beam Irradiation misc Mycosis Fungoides misc Bullous Pemphigoid misc Atypical Lymphocyte
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title_sort	mycosis fungoides bullosa: a case report and review of the literature
title_auth	Mycosis fungoides bullosa: a case report and review of the literature
abstract	Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma. © Kneitz et al; licensee BioMed Central Ltd. 2010
abstractGer	Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma. © Kneitz et al; licensee BioMed Central Ltd. 2010
abstract_unstemmed	Introduction Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma. © Kneitz et al; licensee BioMed Central Ltd. 2010
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