Gupta Anshu, Chaturvedi Sujata, Jha Karuna, Nazir Wazid
Department of Pathology, Institute of Human Behavior and Allied Sciences, New Delhi, India.
Department of Neurosurgery, Guru Teg Bahadur Hospital, New Delhi, India.
Int J Appl Basic Med Res. 2017 Oct-Dec;7(4):269-271. doi: 10.4103/ijabmr.IJABMR_360_16.
Intravascular papillary endothelial hyperplasia (IPEH) also known as Masson's hemangioma is a rare benign reactive vascular lesion of the skin and subcutaneous tissue. It is usually confined to the lumen of preexisting vessels/vascular malformations. It is characterized histologically by papillary fronds lined by proliferating endothelial cells. This lesion is often misinterpreted as soft-tissue tumors and other benign and malignant lesions. We present a case of 13-year-old female with IPEH of scalp causing bony defect because of its rarity and diagnostic challenge, it posed due to nonspecific clinical and radiological findings.
血管内乳头状内皮增生(IPEH),也称为马松血管瘤,是一种罕见的皮肤和皮下组织良性反应性血管病变。它通常局限于先前存在的血管/血管畸形的管腔内。其组织学特征为有增生内皮细胞衬里的乳头状叶。这种病变常被误诊为软组织肿瘤及其他良恶性病变。我们报告一例13岁女性头皮IPEH病例,因其罕见性及诊断挑战(因其非特异性临床和影像学表现所致)导致骨质缺损。