Department of Neurological Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, USA.
J Neurosurg. 2010 May;112(5):978-82. doi: 10.3171/2009.8.JNS081518.
Angiomatoid fibrous histiocytoma (AFH) is a rare soft-tissue neoplasm that most commonly appears in the limbs, typically affecting children and young adults. The tumor has a propensity for local recurrence and recurrent hemorrhage but rarely for remote metastasis. To date, only 2 reports have documented an intracranial occurrence of the tumor (1 of which was believed to be metastatic disease). This is the second report of primary intracranial AFH. Additionally, hemorrhage from an intracranial AFH lesion has yet to be reported, and little is known about the radiographic characteristics and biological behavior of these lesions. In this report, the authors describe the case of a patient with recurrent hemorrhage due to primary multifocal intracranial AFH. Initially misdiagnosed as a cavernous malformation and then an unusual meningioma, the tumor was finally correctly identified when there was a large enough intact resection specimen to reveal the characteristic histological pattern. The diagnosis was confirmed using immunohistochemical and molecular studies.
血管外皮细胞瘤样纤维组织细胞瘤(AFH)是一种罕见的软组织肿瘤,最常发生于四肢,通常影响儿童和青年。该肿瘤具有局部复发和反复出血的倾向,但很少发生远处转移。迄今为止,仅有 2 份文献报道了颅内发生该肿瘤(其中 1 例被认为是转移性疾病)。这是颅内原发 AFH 的第 2 例报告。此外,颅内 AFH 病变的出血尚未见报道,对于这些病变的影像学特征和生物学行为知之甚少。在本报告中,作者描述了 1 例因多发原发性颅内 AFH 反复出血的患者。最初误诊为海绵状血管畸形,然后误诊为一种不常见的脑膜瘤,当有足够大的完整切除标本来显示特征性组织学模式时,最终正确识别了肿瘤。通过免疫组化和分子研究证实了诊断。