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先天自愈性朗格汉斯组织细胞增生症一例 被引量:1

Congenital self-healing Langerhans cell histiocytosis:a case report
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摘要 患儿,女,1个月。头面部红色丘疹、结痂,逐渐增多1个月。皮肤科查体:头皮、额头、躯干、四肢散在黄豆至豌豆大红褐色至黄褐色丘疹、丘疱疹、结痂,部分皮疹少量鳞屑,不易刮除。皮损组织病理示:表皮细胞间水肿,单一核细胞移入,基底细胞液化变性,真皮浅中层较多单一核细胞浸润,细胞核大、胞浆丰富。DIF:表皮细胞间及基底膜带IgG、C3、IgM、IgA阴性。免疫组化:CD1a、S100、CD68弱阳性,Langerin+。未予治疗,随访1个月皮疹基本消退,无新发皮疹。 A one-month-old girl presented with red papules and scabs on her head and face gradually increased for 1 month.Dermatological examination showed soybean to pea sized papules,papulovesicles,scabs on his scalp,forehead,trunk and limbs.A few of the rashes have scales,which were not easily to scrape.Histopathological examination revealed edema between epidermal cells,mononuclear cell migration,basal cell liquefaction and degeneration,more mononuclear cell infiltration in the superficial and middle dermis,with large nucleus and rich cytoplasm.DIF:negative for IgG,C3,IgM,IgA between epidermal cells and basement membrane.Immunohistochemistry:weakly positive for CD1 a,S100,CD68,positive for Langerin.No treatment was given.The lesions dissipated and no new rash occurred after 1 month follow-up.
作者 王娜 吴梅 周桂芝 杨青 WANG Na;WU Mei;ZHOU Guizhi;YANG Qing(Shandong Provincial Hospital for Skin Diseases&Shandong Provincial Institute of Dermatology and Venereology,Shandong First Medical University&Shandong Academy of Medical Sciences,Jinan 250022,China)
出处 《中国麻风皮肤病杂志》 2023年第1期37-39,共3页 China Journal of Leprosy and Skin Diseases
基金 国家自然基金青年基金项目(编号:81903230) 山东省医药卫生科技发展计划项目(编号:202004120262,202004120466)。
关键词 朗格汉斯组织细胞增生症 自愈性 先天性 Langerhans cell histiocytosis self-healing congenital
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  • 1伏利兵,何乐健.郎格罕细胞组织细胞增生症[J].中华病理学杂志,2005,34(11):752-753. 被引量:11
  • 2No auther listed. Histiocytosis syndrurne in ehihh'en. Writing (,roap of Histiocyte Society[ J ]. Lancet, 1987, 1 ( 8526 ): 208-209.
  • 3Schmidt S, Eich G, Geoffray A, et al. Extraosseous langerhans cell histioc-ytosis in chihtren[ J ]. Radiographics, 2008, 28( 3 ): 707-726.
  • 4Wang J, Wu X, Xi ZJ. Langerhans cell histitn:ytosis of bone in chihtren: a clinicopathologic study of 108 cases [J]. World J Pediatr, 2010, 6( 3 ): 255-259.
  • 5Chiong C, Jayachandra S, D Eslick G, et al. A rare case of langerhans cell histiocytosis of the skull in an adult: a systematic review[ J ]. Rare Tumors, 2013, 5( 3 ): e38.
  • 6Querings K, Starz H, Bahta BR. Clinical spectrum of cutaneous langerhans' cell histiocytosis mimicking various diseases [ J ]. Acta Derm Venereot, 2006, 86( 1 ): 39-43.
  • 7Donadieu J, Chalard F, Jeziorski E. Medical management of langerhans cell histincytosis from diagnosis to treatment [ J ]. Expert Opin Pharmaeother, 2012, 13(9): 1309-1322.
  • 8Ahlgrimm-Siess V, Koller S, E1 Shabrawi-Caelen L, et al. New diagnostic methods in dermatopatho[agy: in vivo reflectance confocal micruscopy[ J ]. J Dtsch Dernmtol Ges, 2008, 6(7 ): 591-592.
  • 9Gonzalez S,Gilabcrte-Calzada Y. In vivo reflectance-mode cmlfical microscopy in clinical dermatology and cosmetology [J]. Int J cosmet Sci, 2008, 30( 1 ): 1-17.
  • 10Wurm EM, Curchin CE, Soyer HP. Recent advances in diagnosing cutaneous melanomas [J]. FI000 Med Rep, 2010, 2. pii: 46. doi: 10.3410/M2-46.

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