Results 91 to 100 of about 770 (134)
Indeterminate‐cell histiocytosis: Immunophenotypic and cytogenetic findings in an infant
Medical and Pediatric Oncology, 1999 The authors report the immunohistochemical, ultrastructural, and cytogenetic findings in a case of malignant histiocytic proliferation in an infant.The patient presented initially with bone lesions without skin or systemic involvement. Multiple biopsies were studied extensively by immunohistochemistry and electron microscopy.
Pauline M. Chou +5 more
+6 more sources
British Journal of Dermatology, 1996 An otherwise healthy 50-year-old woman presented with a 6-month history of having developed more than 100 generalized, non-confluent, reddish-brown, partially yellow-coloured papules. A non-epidemotropic, monomorphous infiltrate of vacuolated mononuclear, and occasionally multinuclear, histiocytes, positive for factor XIIIa and macrophage markers HAM56
Bettina G. Zelger +3 more
+6 more sources
Tick bite mimicking indeterminate cell histiocytosis
Pediatric Dermatology, 2017 AbstractTicks are a well‐known vector for viral, bacterial, and rickettsial infections, many of which are accompanied by cutaneous eruptions, but the bite itself can induce a spectrum of inflammatory reactions, including foreign body granuloma, tick bite alopecia, and cutaneous lymphoid hyperplasia.
Thomas Stringer +5 more
openaire +4 more sources
Ocular Involvement in a Case of Systemic Indeterminate Cell Histiocytosis
Cornea, 2001 To describe ocular involvement in a case of systemic indeterminate cell histiocytosis, a rare disease characterized by the proliferation of indistinct histiocytes. These histiocytes resemble Langerhans cells but lack Birbeck granules. The disease usually occurs in adults, with no predisposition for either sex.
Elena Arrondo +5 more
openaire +4 more sources
A Case of Solitary Indeterminate Cell Histiocytosis
The Journal of Dermatology, 2003 Yasuyuki Amo +3 more
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A case of indeterminate cell histiocytosis with ETV3‐NCOA2 translocation
The Journal of DermatologyAbstractIndeterminate cell histiocytosis (ICH) is a rare histiocytic disorder characterized by a proliferation of CD1a+ and CD207/langerin− cells. Recent molecular analyses have identified ETV3‐NCOA2 translocation as a possible aetiopathogenesis of ICH. Herein, we describe the first Japanese case of ICH with ETV3‐NCOA2 translocation.
Norihito Suzuki +9 more
openaire +3 more sources
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Indeterminate Cell Histiocytosis of the Spine: A Case Report
Pediatric Neurosurgery, 2021<b><i>Introduction:</i></b> Indeterminate cell histiocytosis is a rare neoplastic disease characterized by proliferation of dendritic cells that share morphologic and immunophenotypic features of Langerhans cells and non-Langerhans histiocytes.
Roberto J. Perez-Roman +4 more
openaire +2 more sources
Indeterminant Cell Histiocytosis in a Patient With Hemophagocytic Lymphohistiocytosis
The American Journal of Dermatopathology, 2021Abstract: Indeterminant cell histiocytosis is a rare disorder, which often presents as a benign, papular eruption without age or sex predilection. It is diagnosed based on histologic findings that are similar to those seen in Langerhans cell histiocytosis without the characteristic Birbeck granules.
Hannah S, Berman +2 more
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Journal of the European Academy of Dermatology and Venereology, 1995 Marleen Goeteyn
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