Results 121 to 130 of about 9,394 (232)
Histiocytes in nasopharyngeal carcinoma in relation to prognosis [PDF]
, 1986 Hiroaki Nomori +4 more
openalex +1 more source
Histiocytoid Sweet Syndrome With Paradoxical Neutropenia in a Pediatric Patient
Pediatric Dermatology, EarlyView.ABSTRACT Histiocytoid Sweet syndrome (HSS) is a rare inflammatory skin condition characterized by the infiltration of mononuclear cells in the dermis and leukocytosis with neutrophilia. This uncommon variant of classic Sweet syndrome is rarely reported in the literature, especially in pediatric patients.
Shelby Boock +3 more
wiley +1 more source
Unusual immunophenotype displayed by histiocytes in haemophagocytic lymphohistiocystosis. [PDF]
, 1987 Troels Herlin +3 more
openalex +1 more source
Pathology International, EarlyView.Histopathological and immunohistochemical findings from the excisional biopsy of a right parapharyngeal mass in a 56‐year‐old woman with follicular dendritic cell sarcoma arising in Castleman disease. (A) H&E staining reveals atypical tumor cells intimately admixed with lymphocytes. (B) Adjacent areas show “lollipop lesions” characteristic of Castleman
Shunsuke Koga +3 more
wiley +1 more source
Macrophage-histiocytes in malignant lymphoma, small lymphocytic type (well-differentiated lymphocytic lymphoma) [PDF]
, 1985 H. J. Ree +2 more
openalex +1 more source
Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in a ten-year-old girl accompanied by posterior reversible encephalopathy syndrome and disseminated herpes simplex virus infection [PDF]
, 2015 可逆性後頭葉白質脳症は通常臨床的には頭痛・痙攣・視覚障害等の神経症状で発症するしばしば認める疾患である．一方，播種性ヘルペス感染症は免疫不全患者で認める感染症である．今回我々は，EBウイルス関連血球貪食症候群に対するエトポシド・プレドニゾロン・シクロスポリンを用いた多剤併用化学療法中に，シクロスポリン関連可逆性後頭葉白質脳症と播種性ヘルペス感染症と診断された10歳女児を経験したので報告する．EBウイルス関連血球貪食症候群に対する併用療法は当初有効であったが ...
板倉 隆太 +5 more
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First report of indolent cutaneous T‐cell lymphoma in a fennec fox (Vulpes zerda)
Veterinary Dermatology, EarlyView.A 10‐year‐old fennec fox (Vulpes zerda) was presented for multifocal regions of chronic alopecia and crusting. Cutaneous lymphocytosis was diagnosed through histopathological examination and immunohistochemical investigation. Clonal rearrangement of the T‐cell receptor gamma locus supports that lymphocytosis in this case is an indolent lymphoma ...
Kristen L. Shekelle +5 more
wiley +1 more source
Griscelli syndrome : a rare neonatal syndrome [PDF]
, 2006 Griscelli syndrome was first described by Griscelli and Siccardi in 1978 in a hospital in Paris. It is a rare autosomal recessive disorder resulting in pigmentary dilution of the skin and hair, presence of large clumps of pigment in hair shafts and an ...
Calvagna, Victor, Ellul, Marthese
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