Mycosis fungoides and gastric T-cell lymphoma: A case report

被引:2
作者
Scali, Elisabetta [1 ]
Presta, Ivan [1 ]
Donato, Annalidia [2 ]
Schipani, Giusy [1 ]
Dastoli, Stefano [1 ]
Rossi, Marco [3 ]
Mignogna, Chiara [4 ]
Malara, Natalia [3 ]
Nistico, Steven Paul [1 ]
Donato, Giuseppe [1 ]
机构
[1] Magna Graecia Univ Catanzaro, Dept Hlth Sci, Viale Europa Loc, I-88100 Catanzaro, Italy
[2] Magna Graecia Univ Catanzaro, Dept Med & Surg Sci, I-88100 Catanzaro, Italy
[3] Magna Graecia Univ Catanzaro, Dept Clin & Expt Med, I-88100 Catanzaro, Italy
[4] Magna Graecia Univ Catanzaro, Dept Interdipartimental Serv Ctr CIS, I-88100 Catanzaro, Italy
关键词
mycosis fungoides; cutaneous malignant lymphoma; duodenal T-cell lymphoma; sezary syndrome; prognostic value; transformed mycosis fungoides clinical challenges; SMALL-BOWEL OBSTRUCTION; CASTLEMANS-DISEASE; INVOLVEMENT; DIAGNOSIS; FEATURES; PATIENT;
D O I
10.3892/mco.2020.2085
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mycosis fungoides (MF) is a cutaneous malignant lymphoma with an extended clinical course. MF presents in series of dermatological manifestations, beginning with patches and plaques of the skin, and eventually evolving into tumours. Often MF can occur for extended periods without worsening of external symptoms, while the disease advances internally in organs such as lymph nodes, liver, spleen, lung, bone marrow, gastrointestinal tract, pancreas and kidney. The present report presents a clinical case in which gastrointestinal symptomatology occurred a decade after the first dermatological manifestation. Immunohistochemical analysis of the skin, along with small bowel biopsies revealed evidence of gastric T-cell lymphoma. To the best of our knowledge, the present study is the first to describe such a case in the literature.
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页码:1 / 6
页数:6
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