Niechajev I A
Scand J Plast Reconstr Surg. 1982;16(2):183-90. doi: 10.3109/02844318209006589.
Glomus tumours may be either solitary or multiple. The solitary glomus is a quite common, characteristically painful lesion, frequently located under the nails, whereas multiple glomus tumours constitute a rare clinical and genetic entity which is defined by the presence of small bluish intradermal tumours, and autosomal dominant mode of inheritance. The lesions resemble clinically and histologically cavernous hemangioma, but can be differentiated by intraluminar presence of the characteristic glomus cells. Four cases of multiple glomus tumours, one sporadic and three hereditary familial, are reported, and the pedigree of two families with five generations affected by the disease are presented. Radiological investigations of multiple glomus tumours are very sparse, and their results inconsistent. Angiography, venography and thermography did not contribute to diagnosis in the present cases. Skeletal changes associated with multiple glomus tumours are discussed.
血管球瘤可以是单发的或多发的。单发血管球瘤是一种相当常见的、特征性疼痛性病变,常位于指甲下,而多发血管球瘤是一种罕见的临床和遗传实体,其定义为存在小的蓝色皮内肿瘤以及常染色体显性遗传模式。这些病变在临床和组织学上类似于海绵状血管瘤,但可通过管腔内特征性血管球细胞的存在来鉴别。报告了4例多发血管球瘤病例,其中1例为散发性,3例为遗传性家族性,并展示了两个五代受该病影响家庭的系谱。关于多发血管球瘤的放射学研究非常少,且结果不一致。血管造影、静脉造影和热成像在目前的病例中对诊断没有帮助。文中讨论了与多发血管球瘤相关的骨骼变化。