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[非典型部位的孤立性纤维性血管外皮细胞瘤:免疫组化研究的重要性]

[Solitary fibrous hemangiopericytoma of atypical location: importance of immunohistochemical study].

作者信息

Soriano-Hernández María Isabel, Husein-ElAhmed Husein, Ruíz-Molina Inmaculada

机构信息

Departamento de Dermatología. Hospital Clínico San Cecilio, Granada, Spain.

Servicio de Patología, Hospital Infanta Margarita Córdoba, Spain.

出版信息

Cir Cir. 2014 May-Jun;82(3):323-7.

Abstract

BACKGROUND

The rare cutaneous solitary fibrous tumor was initially described in the thoracic cavity in relation to the pleura and subsequently been associated with other serous membranes. It has been described in other extraserosal locations including the skin. Knowledge of its existence along with fairly typical histological features and the immunohistochemical expression pattern with intense positivity for CD34 allow the increasing diagnosis of this condition, which suggests that these cases were not previously diagnosed as such.

CLINICAL CASE

We report the case of a 43 year-old male with a painless nodule in the first left finger pad clinically suggestive of pyogenic granuloma or nodular melanoma, which was diagnosed by excisional biopsy and immunohistochemical study as a solitary fibrous tumor.

DISCUSSION

Only 11 cases of cutaneous solitary fibrous tumor have been published in the following locations: head, cheek, thigh, chest, back and nose. Our work describes the first case of cutaneous solitary fibrous tumor in the hand. The solitary fibrous tumor derived from mesenchymal cells expresses CD34 and hence its presentation in any location. In our case it was in the hand. It explains the problems encountered in the clinical differential diagnosis with other tumors as nodular melanoma, pyogenic granuloma, giant cell tumor of tendon sheath, fibroma, benign peripheral nerve sheath tumors, etc. As we consider the histology, differential diagnosis should be made with other tumors that also express CD34.

CONCLUSIONS

Solitary fibrous tumors derived from mesenchymal cells express CD34 and hence its presentation in any location. In our case it was in the finger pad.

摘要

背景

罕见的皮肤孤立性纤维瘤最初是在胸腔内与胸膜相关联被描述的,随后又与其他浆膜有关。它也在包括皮肤在内的其他浆膜外部位被描述过。了解其存在以及相当典型的组织学特征和免疫组化表达模式(CD34呈强阳性)使得对这种疾病的诊断越来越多,这表明这些病例以前未被如此诊断。

临床病例

我们报告一例43岁男性,其左手中指掌面有一无痛性结节,临床提示为化脓性肉芽肿或结节性黑色素瘤,经切除活检和免疫组化研究诊断为孤立性纤维瘤。

讨论

仅11例皮肤孤立性纤维瘤已发表于以下部位:头部、脸颊、大腿、胸部、背部和鼻子。我们的工作描述了首例手部皮肤孤立性纤维瘤病例。源自间充质细胞的孤立性纤维瘤表达CD34,因此可出现在任何部位。在我们的病例中它出现在手部。这解释了在与其他肿瘤如结节性黑色素瘤、化脓性肉芽肿、腱鞘巨细胞瘤、纤维瘤、良性外周神经鞘瘤等进行临床鉴别诊断时遇到的问题。当考虑组织学时,应与其他也表达CD34的肿瘤进行鉴别诊断。

结论

源自间充质细胞的孤立性纤维瘤表达CD34,因此可出现在任何部位。在我们的病例中它出现在指掌面。

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