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一例发生于足底的获得性平滑肌瘤。

A case of acquired smooth muscle hamartoma on the sole.

作者信息

Lee Deborah, Kim Sang-Hyun, Hong Soon-Kwon, Sung Ho-Suk, Hwang Seon-Wook

机构信息

Department of Dermatology, Busan Paik Hospital, College of Medicine, Inje University, Busan, Korea.

出版信息

Ann Dermatol. 2009 Feb;21(1):78-80. doi: 10.5021/ad.2009.21.1.78. Epub 2009 Feb 28.

Abstract

A smooth muscle hamartoma is a benign proliferation of smooth muscle bundles within the dermis. It arises from smooth muscle cells that are located in arrector pili muscles, dartos muscles, vascular smooth muscles, muscularis mammillae and the areolae. Acquired smooth muscle hamartoma (ASMH) is rare, with only 10 such cases having been reported in the English medical literature to date. Most of these cases of ASMH were shown to have originated from arrector pili and dartos muscles. Only one case was reported to have originated from vascular smooth muscle cells. A 21 year-old woman presented with a tender pigmented nodule, with numbness, on the sole of her foot, and this lesion had developed over the previous 18 months. The lesion showed no hyperpigmentation or hypertrichosis, and the biopsies demonstrated increased smooth muscle bundles in the dermis, and especially around the blood vessels. Moreover, the specimens stained positive with Masson trichrome stain and alpha-smooth-muscle actin antibodies, thus supporting our diagnosis of ASMH of the foot sole. Herein, we report on a rare case of ASMH on the foot sole, and this lesion originated from vascular smooth muscle cells. This type of case has not been previously described in the English medical literature.

摘要

平滑肌瘤是真皮内平滑肌束的良性增生。它起源于位于立毛肌、肉膜肌、血管平滑肌、乳头肌和乳晕的平滑肌细胞。获得性平滑肌瘤(ASMH)较为罕见,迄今为止英文医学文献中仅报道了10例此类病例。这些ASMH病例大多显示起源于立毛肌和肉膜肌。仅1例报道起源于血管平滑肌细胞。一名21岁女性足底出现一个压痛性色素沉着结节,伴有麻木感,该病变在过去18个月内逐渐发展。病变无色素沉着过多或多毛现象,活检显示真皮内平滑肌束增多,尤其是血管周围。此外,标本经Masson三色染色和α-平滑肌肌动蛋白抗体染色呈阳性,从而支持我们对足底ASMH的诊断。在此,我们报告一例罕见的足底ASMH病例,该病变起源于血管平滑肌细胞。这种类型的病例此前在英文医学文献中尚未有描述。

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A case of acquired smooth muscle hamartoma of the scrotum.一例后天性阴囊平滑肌瘤。
Clin Exp Dermatol. 2005 Sep;30(5):523-4. doi: 10.1111/j.1365-2230.2005.01862.x.
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