Musumeci Maria Letizia, Nasca Maria Rita, De Pasquale Rocco, Schwartz Robert A, Micali Giuseppe
Dermatology Clinic, University of Catania, Italy.
Pediatr Dermatol. 2006 May-Jun;23(3):239-42. doi: 10.1111/j.1525-1470.2006.00225.x.
We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous pseudo-vesicular lesions and plaques, as well as verrucous brown papules, were present on the penis and scrotum. The prepuce was hypertrophic, with severe phimosis. Histologic analysis revealed dilated lymphatic vessels lined by a discontinuous layer of flat endothelial cells in the papillary dermis and extending down to the reticular dermis. Dilated blood vessels were also present but no cellular abnormalities were identified. A diagnosis of superficial cutaneous lymphatic malformations was made. To the best of our knowledge, this is the first detailed cutaneous histologic investigation in a patient with Hennekam syndrome. We assume that the onset of cutaneous lesions in our patient was likely triggered by a generalized worsening of his lymphedema.
我们描述了一名16岁男孩,患有肠道淋巴管扩张症、四肢和生殖器淋巴水肿、轻度智力障碍、面部异常(亨内坎综合征)以及皮肤病变。生殖器区域的严重水肿形成了一个巨大肿物,包括阴囊和阴茎。阴茎和阴囊上有许多成簇的红紫色假水疱性病变和斑块,以及疣状褐色丘疹。包皮肥厚,伴有严重包茎。组织学分析显示,乳头真皮层有扩张的淋巴管,由一层不连续的扁平内皮细胞衬里,并延伸至网状真皮层。也存在扩张的血管,但未发现细胞异常。诊断为浅表性皮肤淋巴管畸形。据我们所知,这是对一名亨内坎综合征患者进行的首次详细皮肤组织学研究。我们推测,该患者皮肤病变的发生可能是由其淋巴水肿的全身性恶化引发的。