Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review
Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common,...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Innella, Giovanni [verfasserIn] Miccoli, Sara [verfasserIn] Colussi, Dora [verfasserIn] Pradella, Laura Maria [verfasserIn] Amato, Laura Benedetta [verfasserIn] Zuntini, Roberta [verfasserIn] Salfi, Nunzio Cosimo Mario [verfasserIn] Collina, Guido [verfasserIn] Ferrara, Francesco [verfasserIn] Ricciardiello, Luigi [verfasserIn] Turchetti, Daniela [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2021 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Pathology, research and practice - München : Elsevier, 1978, 218 |
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| Übergeordnetes Werk: |
volume:218 |
| DOI / URN: |
10.1016/j.prp.2020.153339 |
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| 520 | |a Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. | ||
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10.1016/j.prp.2020.153339 doi (DE-627)ELV005504767 (ELSEVIER)S0344-0338(20)32194-4 DE-627 ger DE-627 rda eng 610 DE-600 44.47 bkl Innella, Giovanni verfasserin (orcid)0000-0002-6909-2412 aut Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. Cowden syndrome Gastrointestinal polyposis Colorectal cancer risk Miccoli, Sara verfasserin aut Colussi, Dora verfasserin aut Pradella, Laura Maria verfasserin aut Amato, Laura Benedetta verfasserin aut Zuntini, Roberta verfasserin aut Salfi, Nunzio Cosimo Mario verfasserin aut Collina, Guido verfasserin aut Ferrara, Francesco verfasserin aut Ricciardiello, Luigi verfasserin (orcid)0000-0003-2568-6208 aut Turchetti, Daniela verfasserin aut Enthalten in Pathology, research and practice München : Elsevier, 1978 218 Online-Ressource (DE-627)325789517 (DE-600)2039756-2 (DE-576)094480672 1618-0631 nnns volume:218 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 44.47 Pathologie Medizin AR 218 |
| spelling |
10.1016/j.prp.2020.153339 doi (DE-627)ELV005504767 (ELSEVIER)S0344-0338(20)32194-4 DE-627 ger DE-627 rda eng 610 DE-600 44.47 bkl Innella, Giovanni verfasserin (orcid)0000-0002-6909-2412 aut Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. Cowden syndrome Gastrointestinal polyposis Colorectal cancer risk Miccoli, Sara verfasserin aut Colussi, Dora verfasserin aut Pradella, Laura Maria verfasserin aut Amato, Laura Benedetta verfasserin aut Zuntini, Roberta verfasserin aut Salfi, Nunzio Cosimo Mario verfasserin aut Collina, Guido verfasserin aut Ferrara, Francesco verfasserin aut Ricciardiello, Luigi verfasserin (orcid)0000-0003-2568-6208 aut Turchetti, Daniela verfasserin aut Enthalten in Pathology, research and practice München : Elsevier, 1978 218 Online-Ressource (DE-627)325789517 (DE-600)2039756-2 (DE-576)094480672 1618-0631 nnns volume:218 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 44.47 Pathologie Medizin AR 218 |
| allfields_unstemmed |
10.1016/j.prp.2020.153339 doi (DE-627)ELV005504767 (ELSEVIER)S0344-0338(20)32194-4 DE-627 ger DE-627 rda eng 610 DE-600 44.47 bkl Innella, Giovanni verfasserin (orcid)0000-0002-6909-2412 aut Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. Cowden syndrome Gastrointestinal polyposis Colorectal cancer risk Miccoli, Sara verfasserin aut Colussi, Dora verfasserin aut Pradella, Laura Maria verfasserin aut Amato, Laura Benedetta verfasserin aut Zuntini, Roberta verfasserin aut Salfi, Nunzio Cosimo Mario verfasserin aut Collina, Guido verfasserin aut Ferrara, Francesco verfasserin aut Ricciardiello, Luigi verfasserin (orcid)0000-0003-2568-6208 aut Turchetti, Daniela verfasserin aut Enthalten in Pathology, research and practice München : Elsevier, 1978 218 Online-Ressource (DE-627)325789517 (DE-600)2039756-2 (DE-576)094480672 1618-0631 nnns volume:218 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 44.47 Pathologie Medizin AR 218 |
| allfieldsGer |
10.1016/j.prp.2020.153339 doi (DE-627)ELV005504767 (ELSEVIER)S0344-0338(20)32194-4 DE-627 ger DE-627 rda eng 610 DE-600 44.47 bkl Innella, Giovanni verfasserin (orcid)0000-0002-6909-2412 aut Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review 2021 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. Cowden syndrome Gastrointestinal polyposis Colorectal cancer risk Miccoli, Sara verfasserin aut Colussi, Dora verfasserin aut Pradella, Laura Maria verfasserin aut Amato, Laura Benedetta verfasserin aut Zuntini, Roberta verfasserin aut Salfi, Nunzio Cosimo Mario verfasserin aut Collina, Guido verfasserin aut Ferrara, Francesco verfasserin aut Ricciardiello, Luigi verfasserin (orcid)0000-0003-2568-6208 aut Turchetti, Daniela verfasserin aut Enthalten in Pathology, research and practice München : Elsevier, 1978 218 Online-Ressource (DE-627)325789517 (DE-600)2039756-2 (DE-576)094480672 1618-0631 nnns volume:218 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 44.47 Pathologie Medizin AR 218 |
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Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review |
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Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review |
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Innella, Giovanni |
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Innella, Giovanni Miccoli, Sara Colussi, Dora Pradella, Laura Maria Amato, Laura Benedetta Zuntini, Roberta Salfi, Nunzio Cosimo Mario Collina, Guido Ferrara, Francesco Ricciardiello, Luigi Turchetti, Daniela |
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colorectal polyposis as a clue to the diagnosis of cowden syndrome: report of two cases and literature review |
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Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review |
| abstract |
Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. |
| abstractGer |
Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. |
| abstract_unstemmed |
Cowden Syndrome (CS) is an autosomal dominant disorder characterized by hamartomatous growth in several organs and by an increased risk of malignancies, which makes its recognition essential to undertake risk reduction measures. Although the involvement of gastrointestinal tract is extremely common, awareness of this entity among gastroenterologists appears limited. |
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Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review |
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Miccoli, Sara Colussi, Dora Pradella, Laura Maria Amato, Laura Benedetta Zuntini, Roberta Salfi, Nunzio Cosimo Mario Collina, Guido Ferrara, Francesco Ricciardiello, Luigi Turchetti, Daniela |
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Miccoli, Sara Colussi, Dora Pradella, Laura Maria Amato, Laura Benedetta Zuntini, Roberta Salfi, Nunzio Cosimo Mario Collina, Guido Ferrara, Francesco Ricciardiello, Luigi Turchetti, Daniela |
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