Lehman T D, Morgan T K, Lehman N L, Vogel H, McGuire J S
Department of Dermatology, Stanford University Medical Center, Stanford, CA 94305, U.S.A.
Br J Dermatol. 2004 Dec;151(6):1266-9. doi: 10.1111/j.1365-2133.2004.06267.x.
We report a woman with recessive dystrophic epidermolysis bullosa (RDEB) in whom there was prolonged sepsis and death at age 22 years. Autopsy revealed multiple epidermolytic skin lesions with chronic ulceration, mesangioproliferative glomerulonephritis and multifocal necrotizing leucoencephalopathy (MNL) of the pons. The latter two conditions may have been mediated by sepsis-associated cytokines. Although mesangioproliferative glomerulonephritis has previously been described in association with RDEB, to our knowledge this is the first report of MNL in a patient with RDEB.
我们报告了一名患有隐性营养不良性大疱性表皮松解症(RDEB)的女性,她在22岁时发生了长时间的败血症并死亡。尸检发现多处表皮松解性皮肤病变伴慢性溃疡、系膜增生性肾小球肾炎和脑桥多灶性坏死性白质脑病(MNL)。后两种情况可能是由败血症相关的细胞因子介导的。虽然系膜增生性肾小球肾炎此前已被描述与RDEB相关,但据我们所知,这是首例RDEB患者发生MNL的报告。