Lu Wei, Cao Yan, Zeng Fanhua, Chen Chun, Yang Zhenyu, Qi Zuoliang, Yang Xiaonan
The Department of Hemangioma and Vascular Malformation, Plastic Surgery Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC), Beijing, People's Republic of China.
The Department of Pathology, Plastic Surgery Hospital, Chinese Academy of Medical Sciences (CAMS) and Peking Union Medical College (PUMC), Beijing, People's Republic of China.
Clin Cosmet Investig Dermatol. 2023 Sep 28;16:2697-2719. doi: 10.2147/CCID.S420019. eCollection 2023.
Benign lymphangioendothelioma (BL) is a rare, poorly identified, slow-growing benign vascular lesion characterized by asymptomatic, solitary, well-demarcated macules, or by mildly infiltrated plaque. We report a case of an atypical BL that arose as a tender, protuberant, flesh-colored mass with cyanotic vesicles, and then progressed to a persistent exudative wound after two incomplete excisions. The patient was also diagnosed with thoracic duct narrowing. Although the stenosis was removed by surgery, the right lower extremity ulceration and exudation did not improve. Thus, we performed a thorough excision and split-thickness skin graft transplant following vacuum sealing drainage, and eventually the patient had a favorable functional and cosmetic outcome. A biopsy revealed irregular, dilated vascular spaces lined with a single layer of flat endothelial cells extending from the superficial dermis to the subcutis that did not reach the striated muscles. Additionally, by reviewing the literature on BL, in this paper we summarize the diverse pathogenic, morphological, and immunohistochemical presentations for this rare disease, as well as the histopathological differential diagnosis of lymphangiomatosis, Kaposi's sarcoma, and angiosarcoma.
良性淋巴管内皮瘤(BL)是一种罕见的、难以明确诊断的、生长缓慢的良性血管病变,其特征为无症状的、孤立的、边界清晰的斑疹,或轻度浸润的斑块。我们报告一例非典型BL病例,最初表现为一个有压痛的、突出的、肉色肿物并伴有青紫水疱,在两次不完全切除后进展为持续性渗出性伤口。该患者还被诊断为胸导管狭窄。尽管通过手术解除了狭窄,但右下肢溃疡和渗出并未改善。因此,我们在持续负压封闭引流后进行了彻底切除和中厚皮片移植,最终患者获得了良好的功能和美容效果。活检显示不规则的、扩张的血管腔隙,内衬单层扁平内皮细胞,从浅表真皮延伸至皮下组织,但未累及横纹肌。此外,通过回顾关于BL的文献,我们在本文中总结了这种罕见疾病多样的致病、形态学和免疫组化表现,以及淋巴管瘤病、卡波西肉瘤和血管肉瘤的组织病理学鉴别诊断。