McCormack K, Kaplan D, Murray J C, Fetter B F
Department of Pathology, Duke University Medical Center, Durham, NC 27710.
J Am Acad Dermatol. 1988 Feb;18(2 Pt 2):416-9. doi: 10.1016/s0190-9622(88)70060-2.
Pacinian neurofibromas are unusual tumors with components that resemble Vater-Pacini corpuscles and are probably a variant of nerve-sheath myxoma. Lesions composed predominantly of these structures have occurred on or near the buttocks in three previously reported cases; however, all were solitary and congenital. Two of these patients, with lesions that closely resembled mature Vater-Pacini corpuscles, had underlying skeletal anomalies. Our patient had multiple hairy pacinian neurofibromas (nerve-sheath myxomas) on the buttocks that were not associated with radiographic evidence of and underlying skeletal anomaly. Skeletal anomalies may be associated with "sacrococcygeal paciniomas" but probably not with true pacinian neurofibromas.
帕西尼神经纤维瘤是一种罕见的肿瘤,其成分类似于环层小体,可能是神经鞘黏液瘤的一种变体。在先前报道的3例病例中,主要由这些结构组成的病变发生在臀部或其附近;然而,所有病例均为单发且先天性的。其中2例病变与成熟的环层小体极为相似的患者存在潜在的骨骼异常。我们的患者臀部有多个毛发状帕西尼神经纤维瘤(神经鞘黏液瘤),但影像学检查未发现潜在的骨骼异常证据。骨骼异常可能与“骶尾部帕西尼瘤”有关,但可能与真正的帕西尼神经纤维瘤无关。