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苔藓样、糜烂性和溃疡性皮肤纤维瘤。另外三种临床病理变体。

Lichenoid, erosive and ulcerated dermatofibromas. Three additional clinico-pathologic variants.

作者信息

Sánchez Yus E, Soria L, de Eusebio E, Requena L

机构信息

Department of Dermatology of the Hospital Clínico San Carlos, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

出版信息

J Cutan Pathol. 2000 Mar;27(3):112-7. doi: 10.1034/j.1600-0560.2000.027003112.x.

Abstract

On the occasion of a case of dermatofibroma with histological lichenoid features, we reviewed from our files all the cases in which the epidermis, usually hyperplastic in dermatofibroma, was, in some way, partially or completely destroyed. Among a total of 484 dermatofibromas, we found three lichenoid, six erosive and two ulcerated cases. In the three lichenoid cases, the columnar epidermal basal cells were lacking (squamotization of the basal layer) and in two of them there was a cleft between the epidermis and the dermatofibroma. Three of the six eroded cases were large pedunculated dermatofibromas with inflammatory phenomena of variable intensity. One case was in the center of a plaque of lichen simplex chronicus with some eroded area. In the other two cases, as well as in the two ulcerated lesions, neither inflammation nor epidermal changes usually attributed to rubbing or scratching were seen. Only in three of the eleven cases dermatofibroma was proposed (with question mark) as a clinical diagnosis. Both follow-up and histopathology supported the benign nature of these cases. We may conclude that: i) Lichenoid, erosive and ulcerated changes in dermatofibroma are infrequent phenomena which may make a clinical diagnosis difficult; and ii) in the presence of an otherwise histopathologically typical dermatofibroma, erosion and ulceration should not be considered as suspicious of malignancy.

摘要

在遇到一例具有组织学苔藓样特征的皮肤纤维瘤时,我们从档案中查阅了所有表皮(在皮肤纤维瘤中通常增生)以某种方式部分或完全被破坏的病例。在总共484例皮肤纤维瘤中,我们发现3例苔藓样、6例糜烂性和2例溃疡性病例。在3例苔藓样病例中,柱状表皮基底细胞缺失(基底层鳞状化生),其中2例表皮与皮肤纤维瘤之间有裂隙。6例糜烂性病例中有3例是带蒂的大皮肤纤维瘤,伴有不同程度的炎症现象。1例位于慢性单纯性苔藓斑块中央,有一些糜烂区域。在另外2例病例以及2例溃疡性病变中,未见通常归因于摩擦或搔抓的炎症或表皮改变。在11例病例中,只有3例皮肤纤维瘤(带问号)被提出作为临床诊断。随访和组织病理学均支持这些病例的良性性质。我们可以得出结论:i)皮肤纤维瘤中的苔藓样、糜烂性和溃疡性改变是罕见现象,可能会使临床诊断困难;ii)在存在其他方面组织病理学典型的皮肤纤维瘤时,糜烂和溃疡不应被视为恶性可疑。

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