Wu K.-H.Dai Y.-S.Tsai M.-J.Lin S.-C.Wang L.-H.Huang M.-T.BOR-LUEN CHIANG2021-07-022021-07-0220000253-2662https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034030269&partnerID=40&md5=4fad28df3780c8649b5cf9a04c58b805https://scholars.lib.ntu.edu.tw/handle/123456789/568088Lichen sclerosus et atrophicus (LSA) rarely coexists with morphea, especially when bullae occur in lesions of morphea. Here we report the case of a 15-year-old girl with this condition, who also fulfilled four out of 11 diagnostic criteria for systemic lupus erythematosus (SLE). Tissue biopsy of different skin lesions showed LSA in the regions of bullous morphea, that has rarely been reported in the literature.Bullous morphea; Lichen sclerosus et atrophicus (LSA); Systemic lupus erythematosus (SLE)[SDGs]SDG3azathioprine; hydrocortisone; naproxen; prednisolone; urea; adolescent; antibody titer; article; bullous skin disease; case report; female; histopathology; human; human tissue; lichen sclerosus et atrophicus; lupus erythematosus; morphea; skin biopsy; systemic lupus erythematosus; Adolescent; Female; Humans; Lichen Sclerosus et Atrophicus; Lupus Erythematosus, Systemic; Scleroderma, Localizedjournal article108069662-s2.0-0034030269