Dermatomyositis panniculitis: a clinicopathological and immunohistochemical study of 18 cases

被引:23
作者
Santos-Briz, A. [1 ]
Calle, A. [2 ]
Linos, K. [3 ,4 ]
Semans, B. [5 ]
Carlson, A. [6 ]
Sangueza, O. P. [7 ,8 ]
Metze, D. [9 ]
Cerroni, L. [10 ]
Diaz-Recuero, J. L. [11 ]
Alegria-Landa, V. [11 ]
Mascaro, J. M. [12 ]
Moreno, C. [13 ]
Rodriguez-Peralto, J. L. [14 ]
Requena, L. [11 ]
机构
[1] Hosp Clin Univ, Dept Pathol, Salamanca, Spain
[2] Hosp Univ & Politecn La Fe, Dept Dermatol, Valencia, Spain
[3] Dartmouth Hitchcock Med Ctr, Dept Pathol & Lab Med, Lebanon, NH 03766 USA
[4] Geisel Sch, Lebanon, NH USA
[5] Semans Dermatopathol Serv, Rochester, IL USA
[6] Albany Med Coll, Dept Pathol & Lab Med, Albany, NY 12208 USA
[7] Wake Forest Univ, Dept Dermatol, Winston Salem, NC 27109 USA
[8] Wake Forest Univ, Dept Pathol, Winston Salem, NC 27109 USA
[9] Univ Munster, Dept Dermatol, Munster, Germany
[10] Med Univ Graz, Dermatopathol Res Unit, Graz, Austria
[11] Univ Autonoma, Dept Dermatol Fundac Jimenez Diaz, Madrid, Spain
[12] Univ Barcelona, Hosp Clin & Prov, Dept Dermatol, Barcelona, Spain
[13] Univ Alcala de Henares, Hosp Ramon & Cajal, Dept Pathol, Madrid, Spain
[14] Univ Complutense, Hosp Octubre 12, Dept Pathol, Madrid, Spain
关键词
T-CELL LYMPHOMA; JUVENILE DERMATOMYOSITIS; CALCIFIC PANNICULITIS; POLYMYOSITIS; HISTOPATHOLOGY; MANIFESTATION; FEATURES;
D O I
10.1111/jdv.14932
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BackgroundPanniculitis occurring in dermatomyositis is uncommon, with only a few cases described in the literature, most of them as case reports. ObjectiveThis report describes the clinicopathological and immunohistochemical findings in a series of 18 patients with panniculitis associated with dermatomyositis. MethodsIn each patient, we collected the clinical data of the cutaneous lesions as well as the characteristic clinical and laboratory findings. A series of histopathologic findings was recorded in the biopsy of each patient. A panel of antibodies was used in some cases to investigate the immunophenotype of the infiltrate. Data of treatment and follow-up were also collected. ResultsOf the 18 patients, 13 were female and 5 were male, ranging in age from 13 to 74 years (median, 46.4 years). In addition to panniculitis, all patients presented pathognomonic cutaneous findings of DM and reported proximal muscle weakness prior to the diagnosis of panniculitis. Muscle biopsy was performed in 17 patients and MRI in one, all with the diagnosis of inflammatory myopathy. None of the patients presented any associated neoplasia. Panniculitis lesions were located in the upper or lower limbs. Histopathology showed a mostly lobular panniculitis with lymphocytes as the main component of the infiltrate. Most cases showed also numerous plasma cells and lymphocytes surrounding necrotic adipocytes (rimming) were frequently seen. Lymphocytic vasculitis and abundant mucin interstitially deposited between collagen bundles of the dermis were also frequent findings. Late-stage lesions showed hyaline necrosis of the fat lobule and calcification. Immunohistochemistry demonstrated that most lymphocytes of the infiltrate were T-helper lymphocytes, with some B lymphocytes in the lymphoid aggregates and small clusters of CD-123-positive plasmacytoid dendritic cells in the involved fat lobule. ConclusionPanniculitis in dermatomyositis is rare. Histopathologic findings of panniculitis dermatomyositis are identical to those of lupus panniculitis. Therefore, the final diagnosis requires clinic-pathologic correlation. Linked article: This article is commented on by A. Kuhn, pp. 1231-1232 in this issue. To view this article visit
引用
收藏
页码:1352 / 1359
页数:8
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