Langerhans Cell Histiocytosis Presented as Generalized Vesiculo-Pustules in a Neonate
نویسندگان
چکیده
A one-month-old female baby had been noted to have multiple vesicles and pustules over the head, face, trunk and four extremities since she was one-week-old. Under the impression of disseminated herpes virus infection, intravenous acyclovir was given after admission. Serum herpes simplex virus and varicella zoster virus enzyme-linked immunosorbent assay test and virus culture were all fruitless, although herpes simplex virus-1 was vaguely identifi ed in direct fl uorescent staining of lesion scrapings. Unfortunately, new lesions still continued popping out despite treatment. Dermatologist was then consulted, and Tzanck smear as well as skin biopsy were performed. The histopathological exam showed Langerhans cell histiocytosis. Skull x-ray fi lm showed expansile osteolytic lesion over the left parietal area and the chest x-ray increased reticulonodular infi ltration in both lung fi elds. There was no abnormal fi nding in the long bone survey or abdominal sonography. In summary, we report a case of neonatal Langerhans cell histiocytosis presenting as generalized vesiculo-pustules. It should be differentiated from herpes virus infection in the clinical setting. (Dermatol Sinica 27: 176-180, 2009)
منابع مشابه
BRAF V600E-Positive Multisite Langerhans Cell Histiocytosis in a Preterm Neonate
Hemorrhagic pustules with a "blueberry muffin" appearance accompanied by respiratory failure in a neonate present a challenging differential diagnosis that includes infections and neoplasms. We present a case of multiorgan, multisite Langerhans cell histiocytosis (LCH), positive for the oncogenic BRAF V600E mutation, in a preterm neonate. Infants with LCH pose a diagnostic challenge due to thei...
متن کاملGeneralized eruptive histiocytosis: A case report
The histiocytoses are a group of proliferative disorders of themonocyte-macrophage lineage that are neoplastic or reactive innature. Based on immunophenotyping and electron microscopy,two main groups have been recognized namely 1) Langerhanscell histiocytosis (LCH) and 2) non- Langerhans cell histiocytosis(non-LCH). In this study, a fairly rare disease of the non-LCHgroup, generalized eruptive ...
متن کاملLangerhans cell Histiocytosis: Seborrheic dermatitis-like skin signs and polypoid lesion of external ear in a 41-year-old man (Case report)
Langerhans cell histiocytosis includes a broad spectrum of clinical diseases resulted from proliferation and tissue infiltration of differentiated langerhans cells. This term includes Letterer-siwe disease, Hand-Schuller-Christian disease, eosinophilic granuloma and congenital reticulohistiocytosis that are more common in children than adults. This entity has recently been classified into restr...
متن کاملIndeterminate cell histiocytosis: a case report
Indeterminate cell histiocytosis is a very rare proliferative disorderof histiocytes which displays both langerhans cell histiocytosisand non langerhans cell histiocytosis immunophenotypic features.The majority of the patients develop multiple lesions which areclinically indistinguishable from generalized eruptive histiocytosis.We report a 14-year-old girl with multiple papules on the face,scal...
متن کاملLangerhans cell Histiocytosis: Report of a case with cutaneous lesions with favorable response to oral Thalidomide
We report of a 29-year-old man presented with yellow-red, scaling papules on the skin of scalp, retro-auricular folds, inguinal, axillary, chest and abdomen. The lesions had a poikilodermatious appearance in some areas, such as trunk. The patient also had diabetes insipidus and skull osteolytic lesions. The diagnosis of langerhans cell histiocytosis (LCH) was suggested based on H and E staining...
متن کامل