Results 41 to 50 of about 24,507 (317)

A Previously Unrecognized Granulomatous Variant of Gamma-Delta T-Cell Lymphoma

open access: yesDermatopathology, 2021
Primary cutaneous γδ T-cell lymphoma (PCGD-TCL) is an extremely rare and aggressive T-cell neoplasm with complex heterogeneity. We present a series of two patients who presented with firm, subcutaneous nodules and were diagnosed with PCGD-TCL.
Tatsiana Pukhalskaya   +3 more
doaj   +1 more source

A hemophagocytic lymphohistiocytosis case with newly defined UNC13D (C.175G>C; p.Ala59Pro) mutation and a rare complication [PDF]

open access: yes, 2015
Hemophagocytic lymphohistiocytosis (HLH) represents a severe hyperinflammatory condition with cardinal symptoms of prolonged fever, cytopenias, hepatosplenomegaly, and hemophagocytosis by activated, morphologically benign macrophages with impaired ...
Akpınar, Funda Özgürler   +7 more
core   +2 more sources

Os histiócitos e as histiocitoses não Langerhans em dermatologia Histiocytes and non-Langerhans cell histiocytoses in dermatology

open access: yesAnais Brasileiros de Dermatologia, 2003
Atualmente, os histiócitos não são mais compreendidos como células únicas, mas como um grupo heterogêneo de células com o mesmo aspecto histológico, mas com características e funções distintas entre si.
Flávio Barbosa Luz   +3 more
doaj   +1 more source

Granular cell tumor in the pulmonary tree

open access: yesRespiratory Medicine Case Reports, 2022
Granular cell tumors are often benign growths of the tongue, dermis, and subcutaneous tissues. Rarely, we see production in the pulmonary system. These schwannian and histiocyte origin tumors in the lungs are called pulmonary granulocyte tumors.
Nicholas Nassif   +3 more
doaj   +1 more source

Pediatric Liver Transplantation: Then and Now [PDF]

open access: yes, 2020
This paper reviews the past 50 years of liver transplantation in children from the perspective of patient demographics, perioperative patient management, surgical techniques, immunosuppression and patient ...
Banh, DPT   +4 more
core   +1 more source

T-cell/histiocyte-rich large B-cell lymphoma presenting as a primary central nervous system lymphoma

open access: yesRare Tumors, 2015
Primary central nervous system (PCNSL) lymphoma is an aggressive extranodal non-Hodgkin lymphoma, and most cases are classified as diffuse large B-cell lymphoma (DLBCL) by histology.
Pooja Advani   +6 more
doaj   +1 more source

Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms. [PDF]

open access: yesPLoS ONE, 2015
Human chromosomal region 13q14 is a deletion hotspot in prostate cancer, multiple myeloma, and chronic lymphocytic leukemia. This region is believed to host multiple tumor suppressors. Chromosome Condensation 1-like (CHC1L) is located at 13q14, and found
David R Spillane   +9 more
doaj   +1 more source

Myxoid angiomatoid fibrous histiocytoma. report of an uncommon neoplasm with a literature review

open access: yesAdvances in Medical, Pharmaceutical and Dental Research, 2022
Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor usually seen in the extremities of children and adolescents. Classically AFH presents as a painless cystic mass that shows blood filled spaces on cut section and bland histiocyte-like ...
Marwa Mohamed Abd El Aziz   +2 more
doaj   +1 more source

Pancreatic T/histiocyte-rich large B-cell lymphoma: A case report and review of literature

open access: yesWorld Journal of Gastroenterology, 2017
Primary pancreatic lymphoma (PPL) is an extremely rare form of extranodal malignant lymphoma. The most common histological subtype of PPL is diffuse large B cell lymphoma (DLBCL).
Shumei Zheng   +9 more
semanticscholar   +1 more source

Primary Hemophagocytic Lymphohistiocytosis in a Newborn Child

open access: yesZdorovʹe Rebenka, 2014
The article presents the data of clinical observation of hemophagocytic lymphohistiocytosis in newborn child, complicated with spontaneous splenic rupture. Issues of diagnosis according to the recommendations of the International society for the study of
A.I. Kozhemyaka   +7 more
doaj   +1 more source

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