Shahid Sumreen, Khan Maria, Qadar Laila Tul, Akmal Manahil, Jamal Ammarah
Miscellaneous, Civil Hospital Karachi, Karachi, PAK.
Internal Medicine, Dow University of Health Sciences, Karachi, PAK.
Cureus. 2019 May 7;11(5):e4604. doi: 10.7759/cureus.4604.
Rowell syndrome (RS) is a rare entity that presents with lupus erythematosus (LE), erythema multiforme (EM) like lesions and characteristic immunological findings including positive rheumatoid factor (RF), speckled antinuclear antibody (ANA) and positive anti-Ro or anti-La antibodies in the serum. Only a few cases have been reported in the literature, mostly in middle-aged women. Our case is about an 11-year-old male child who had a history of pustular rashes over the whole body with scattered targetoid lesions for the past few months and later developed respiratory distress and swelling of the body. He was extensively investigated and confirmed on specific positive immunochemistry markers as RS along with lobar pneumonia (LP) and lupus nephritis. The co-existence of lobar pneumonia in our patient was a unique feature that has not been previously reported.
罗威尔综合征(RS)是一种罕见的疾病,表现为红斑狼疮(LE)、多形红斑(EM)样皮损以及特征性的免疫学表现,包括血清中类风湿因子(RF)阳性、斑点型抗核抗体(ANA)阳性以及抗Ro或抗La抗体阳性。文献中仅报道了少数病例,大多为中年女性。我们的病例是一名11岁男性儿童,在过去几个月里有全身脓疱性皮疹伴散在靶形皮损的病史,随后出现呼吸窘迫和身体肿胀。他经过广泛检查,通过特异性阳性免疫化学标志物确诊为RS,同时合并大叶性肺炎(LP)和狼疮性肾炎。我们患者中大叶性肺炎的并存是一个此前未被报道过的独特特征。