Syringotropic Mycosis Fungoides: A Rare Variant of the Disease With Peculiar Clinicopathologic Features

被引:45
|
作者
Pileri, Alessandro [1 ,2 ]
Facchetti, Fabio [3 ]
Ruetten, Arno [6 ]
Zumiani, Giuseppe [4 ]
Boi, Sebastiana [5 ]
Fink-Puches, Regina [1 ]
Cerroni, Lorenzo [1 ]
机构
[1] Med Univ Graz, Dept Dermatol, Res Unit Dermatopathol, A-8036 Graz, Austria
[2] Univ Bologna, Div Dermatol, Dept Internal Med Geriatr & Nephrol, I-40126 Bologna, Italy
[3] Univ Spedali Civili Brescia, Dept Pathol, Brescia, Italy
[4] Presidio Osped S Chiara, Dept Dermatol, Trento, Italy
[5] Presidio Osped S Chiara, Dept Dermatopathol, Trento, Italy
[6] Dermatopathol Gemeinschaftslab, Friedrichshafen, Germany
关键词
mycosis fungoides; syringotropic mycosis fungoides; cutaneous T-cell lymphoma; syringolymphoid hyperplasia with alopecia; pilotropic mycosis fungoides; folliculotropic mycosis fungoides; T-CELL LYMPHOMA; OF-THE-LITERATURE; SYRINGOLYMPHOID HYPERPLASIA; FOLLICULAR MUCINOSIS; ECCRINE GLAND; CUTANEOUS LYMPHOMAS; SJOGRENS-SYNDROME; ALOPECIA; ANHIDROSIS; CLASSIFICATION;
D O I
10.1097/PAS.0b013e3182036ce7
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A rare variant of mycosis fungoides (MF) characterized by prominent involvement of the eccrine glands with syringometaplasia has been reported in the past as "syringolymphoid hyperplasia with alopecia," " syringotropic cutaneous T-cell lymphoma," " adnexotropic T-cell lymphoma," or " syringotropic MF." The clinicopathologic features of this variant are not well understood, and only a few case reports or small series have been published to date. We reviewed the clinicopathologic features of 14 patients with syringotropic MF (male: female - 10: 4; median age, 59 years; mean age, 57.8; age range, 33 to 83 y). Six patients had variably large, solitary patches or plaques, located on the thigh (n = 3), arm, trunk, or eyebrow (1 each). The other 8 patients had multiple, mostly generalized lesions. A history of MF was known in 4 of these 8 patients. With the exception of 1 biopsy specimen that was too superficial and did include the eccrine secretory coils but not the eccrine glands, all cases showed prominent involvement of the eccrine glands. Variable degrees of syringometaplasia ranging from small to large epithelial complexes were present in all specimens. The eccrine glands and syringometaplastic structures were surrounded by dense lymphoid infiltrates with prominent epitheliotropism. Concomitant involvement of the epidermis and of the hair follicles was observed in 13 and 8 biopsies, respectively. This is the largest series of syringotropic MF, showing that this is a rare variant of the disease with peculiar clinicopathologic features. Dermatologists and dermatopathologists should be aware of this rare variant of MF to avoid delayed diagnosis and treatment.
引用
收藏
页码:100 / 109
页数:10
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