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Eccrine angiomatous hamartoma, with verrocous hemangioma-like features: A case report

机译:内分泌性血管瘤错构瘤,具有血管样血管瘤特征:1例病例报告

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Eccrine angiomatous hamartoma (EAH) is a rare, benign cutaneous tumor. It is characterized by the proliferation of the eccrine gland elements that are closely associated with capillary proliferation. Patients usually present with a solitary nodule on the extremities that appeared at birth or during the prepubertal years. We report a rare case of EAH in a 13-year-old boy, with clinical features suggesting melanoma. Histologically, an EAH with changes resembling a verrucous hemangioma was noted. Keywords: angiomatous hamartoma, eccrine glands, verrucousIntroductionEccrine angiomatous hamartoma (EAH) is a rare benign neoplasia characterized by the proliferation of the secretory portions of the eccrine glands associated with capillary angiomatosis and proliferation in other elements, such as in the adipose tissue, hair and epidermis. ~((1)) Most cases occur at birth or in early childhood, with various forms of clinical presentation, ranging from simple angiomatous nodules to erythematous-purpuric plaques. Multiple lesions may occur, but the predominant picture is a solitary lesion.Case reportA 13-year-old boy presented with a skin lesion on the right ankle since birth. There was mild pain, but no hyperhidrosis was noted. His medical and family histories were unremarkable. Physical examination revealed a 1.5 cm raised keratotic, dark- brown plaque overlying a 3 cm light brown to bluish, ill-defined plaque on the right ankle. The lesion was excised with clinical suspicion of melanoma.The histological examination of the excised biopsy showed a hyperkeratotic verrucous surface, with numerous dilated capillaries in the papillary dermis (Fig. 1) Open in a separate windowFig. (1) Hyperkeratosis, papillomatosis, and blood vessel proliferation in the superficial dermis (H&E, ×200).
机译:内分泌血管瘤错构瘤(EAH)是一种罕见的良性皮肤肿瘤。其特征在于与毛细血管增生密切相关的内分泌腺元素的增生。患者通常在出生时或青春期前的四肢出现孤立性结节。我们报告了一个13岁男孩的EAH罕见病例,临床特征提示黑色素瘤。从组织学上讲,有一种EAH,其变化类似于疣状血管瘤。关键字:血管瘤性错构瘤,外分泌腺,疣状引言内分泌血管瘤性错构瘤(EAH)是一种罕见的良性肿瘤,其特征是与毛细血管血管瘤相关的内分泌腺分泌部分增生以及其他成分(例如脂肪组织,头发和皮肤)的增生。表皮。 〜((1))大多数病例发生在出生或儿童早期,临床表现形式多样,从简单的血管瘤到红斑和紫癜。可能发生多处病变,但主要表现为孤立病变。病例报告自出生以来,一名13岁男孩在右脚踝出现皮肤病变。有轻度疼痛,但未见多汗症。他的病史和家族史并不多见。体格检查发现,右脚踝上有一个1.5厘米升高的角化,深棕色斑块,上面覆盖着3厘米浅棕色至蓝色,界限不清的斑块。病灶切除后,临床上怀疑有黑色素瘤。切除的活检组织学检查显示,角化过度的疣状表面,乳头状真皮中有许多扩张的毛细血管(图1)在单独的窗口中打开。 (1)浅表层真皮过度角化,乳头状瘤和血管增生(H&E,×200)。

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