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恶性组织细胞增多症的皮肤受累。病例报告及文献复习。

Cutaneous involvement in malignant histiocytosis. Case report and review of the literature.

作者信息

Marshall M E, Farmer E R, Trump D L

出版信息

Arch Dermatol. 1981 May;117(5):278-81.

PMID:7224656
Abstract

Malignant histiocytosis (MH) is a rare, malignant neoplasm with protein manifestations, including fever, lymphadenopathy, hepatosplenomegaly, pancytopenia, and, infrequently, cutaneous lesions. A patient had initial manifestations that included fever and skin lesions. Skin lesions began on distal areas of the extremities and spread to involve proximal areas of the extremities and the abdomen. Erythematous maculopapular lesions, nodules, and plaques were present in various stages of development, which evolved into ulcerated plaques that exuded a serosanguineous discharge. Spontaneous healing of lesions occurred, leaving hyperpigmented, atrophic scars. Histologically, the deep dermis and subcutaneous tissues contained a diffuse infiltrate of histiocytes, lymphocytes, and mononuclear cells. Erythrophagocytosis by histiocytes was present in the skin biopsy material. Thirteen percent of 320 cases in the literature had skin involvement. This report and review of the literature indicate that, in selected cases, skin biopsy may contribute to the diagnosis of MH.

摘要

恶性组织细胞增多症(MH)是一种罕见的恶性肿瘤,有多种临床表现,包括发热、淋巴结病、肝脾肿大、全血细胞减少,以及偶尔出现的皮肤病变。一名患者最初的表现包括发热和皮肤病变。皮肤病变始于四肢远端,随后蔓延至四肢近端和腹部。红斑丘疹性病变、结节和斑块处于不同的发展阶段,进而演变成溃疡斑块,伴有血清样血性渗出物。病变可自发愈合,留下色素沉着、萎缩性瘢痕。组织学检查显示,真皮深层和皮下组织有组织细胞、淋巴细胞和单核细胞的弥漫性浸润。皮肤活检材料中可见组织细胞吞噬红细胞现象。文献中320例病例中有13%出现皮肤受累。本报告及文献综述表明,在某些病例中,皮肤活检可能有助于MH的诊断。

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