Results 41 to 50 of about 24,352 (312)

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

Acute leukemia in association with Langerhans cell histiocytosis [PDF]

open access: yes, 1994
Langerhans cell histiocytosis (LCH) and malignancy occurring in the same individual is unusual and has generally been the subject of isolated case reports.
Aricò, M. (Maurizio)   +5 more
core   +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

Atypical Histiocyte-Rich Sweet’s Syndrome

open access: yesCase Reports in Dermatological Medicine, 2017
Sweet’s Syndrome is a rare neutrophilic dermatosis thought to be a result of immune dysregulation occurring in the setting of drug exposure, recent infection, pregnancy, and underlying malignancy or idiopathic with specific and widely accepted diagnostic
Sharon Chi   +4 more
doaj   +1 more source

Primary oral manifestation of Langerhans cell histiocytosis refractory to conventional therapy but susceptible to BRAF-specific treatment: a case report and review of the literature [PDF]

open access: yes, 2019
Langerhans cell histiocytosis (LCH) is a diagnostic and therapeutic challenge. We report on a rare case of its primary oral manifestation that was treated successfully with the BRAF-specific agent, vemurafenib, after insufficient standard LCH treatment ...
Beck-Broichsitter, Benedicta   +8 more
core   +1 more source

Immune myopathy with large histiocyte-related myofiber necrosis

open access: yesNeurology, 2019
Objective To describe the features of a new, pathologically distinctive, acquired myopathy with an unusual pattern of scattered necrotic muscle fibers that are neighbored, surrounded, or invaded, by large, often multinucleated, histiocytic cells. Methods
A. Pestronk   +5 more
semanticscholar   +1 more source

Recurrent temporal bone tenosynovial giant cell tumor with chondroid metaplasia: the use of imaging to assess recurrence [PDF]

open access: yes, 2014
Tenosynovial giant cell tumor (TGCT) is a benign proliferative lesion of unclear etiology. It is predominantly monoarticular and involves the synovium of the joint, tendon sheath, and bursa.
Fernandez, M.   +6 more
core   +1 more source

Case report: Complete clinical remission of feline progressive histiocytosis after multimodal treatment including electrochemotherapy

open access: yesFrontiers in Veterinary Science
Feline histiocytic diseases are uncommon and rarely reported. Feline progressive histiocytosis (FPH) is the most common histiocytic disease in cats, predominantly affecting middle-aged animals.
Bruna Voltolin de Sena   +8 more
doaj   +1 more source

Recurrent adult-onset hypophyseal Langerhans cell histiocytosis after radiotherapy: A case report [PDF]

open access: yes, 2012
INTRODUCTION: Langerhans cell histiocytosis is a rare disease within the adult population, with very few cases reported as solitary hypophyseal lesions in adults.
Chicoine, Michael R   +8 more
core   +2 more sources

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