Unilesional mycosis fungoides: a case report and review of literature

Wasim Selimul Haque, Shakibul Alam, H. Kabir, Al-Amin Chowdhury
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Abstract

Mycosis fungoides (MF) is the commonest primary cutaneous T-cell lymphoma (CTCL). Classically MF is presented clinically as multilesional disease but occurrence of solitary lesion, though quite rare, is on the record. This rare variant of MF is clinically and histopathologically indistinguishable from classic MF. Due to the rarity of the presentation the clinician may miss the diagnosis and the pathologist may also be in diagnostic dilemma specially if not clinically oriented. Here we describe a case of unilesional/solitary MF (UMF) in a 59 years old male who was initially clinically diagnosed as inflammatory dermatosis and was treated accordingly without any appreciable clinical response for over 4 years. Unresponsiveness to empirical treatment led to biopsy which finally proved it to be UMF. The clinical, light microscopic and immunohistochemical features of UMF are briefly reviewed to create awareness among the clinicians and pathologists about this rare variant of MF. IMC J Med Sci 2022; 16(1): 006 *Correspondence: Wasim Selimul Haque, Head, Department of Histopathology and Cytopathology, Jaber Al-Ahmed Armed Forces Hospital, Kuwait Armed, Forces, Subhan Cantonment, Kuwait. Email: audrirodelawasim@gmail.com
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单发蕈样真菌病1例报告及文献复习
蕈样真菌病是最常见的原发性皮肤t细胞淋巴瘤(CTCL)。典型的MF临床表现为多病变,但单发病变的发生虽然很少见,但也有记录。这种罕见的MF变型在临床和组织病理学上与典型MF难以区分。由于罕见的表现,临床医生可能会错过诊断,病理学家也可能处于诊断困境,特别是如果没有临床导向。在这里,我们描述了一个59岁男性的单发/孤立性MF (UMF)病例,他最初被临床诊断为炎症性皮肤病,并接受了相应的治疗,但在4年多的时间里没有任何明显的临床反应。对经验治疗无反应导致活检,最终证明它是UMF。本文简要回顾了UMF的临床、光镜和免疫组织化学特征,以提高临床医生和病理学家对这种罕见MF变异的认识。中华医学会医学杂志2022;16(1): 006*通信:科威特Subhan军营Jaber Al-Ahmed武装部队医院组织病理学和细胞病理学科主任Wasim Selimul Haque。电子邮件:audrirodelawasim@gmail.com
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审稿时长
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