骨内乳头状淋巴管内血管内皮瘤(PILA):一例新病例及文献复习。

Clinical Sarcoma Research Pub Date : 2018-01-30 eCollection Date: 2018-01-01 DOI:10.1186/s13569-018-0087-9
Marco Gambarotti, Alberto Righi, Marta Sbaraglia, Giuseppe Bianchi, Piero Picci, Daniel Vanel, Angelo Paolo Dei Tos
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引用次数: 13

摘要

背景:乳头状淋巴管内血管内皮瘤(PILA)是一种局部侵袭性,很少转移的血管肿瘤,通常发生在软组织,文献中报道的病例不到40例,仅报道了3例骨。病例介绍:我们描述了一个51岁的男性病例,他的左锁骨近端骨内PILA和其他两个影像学上明显的病变。患者接受锁骨病灶边缘切除治疗,但术后1个月未随访。结论:PILA也可以发生在骨骼中,尽管非常罕见,并且必须在血管骨肿瘤的鉴别诊断中加以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intraosseous papillary intralymphatic angioendothelioma (PILA): one new case and review of the literature.

Intraosseous papillary intralymphatic angioendothelioma (PILA): one new case and review of the literature.

Intraosseous papillary intralymphatic angioendothelioma (PILA): one new case and review of the literature.

Background: Papillary intralymphatic angioendothelioma (PILA) is a locally aggressive, rarely metastasizing vascular tumor, generally occurring in the soft tissues, with less than 40 cases described in the literature and only three cases reported in bone.

Case presentation: We describe the case of a 51-year-old male with an intraosseous PILA of the proximal edge of his left clavicle and two other lesions evident on imaging. The patient was treated with marginal resection of the clavicle lesion but was lost to follow-up 1 month after surgery.

Conclusions: PILA can also occur in bone, albeit very rarely, and has to be considered in the differential diagnosis of vascular bone tumors.

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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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