Results 81 to 90 of about 9,012 (189)
Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]
The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg+5 more
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Multiple cutaneous reticulohistiocytoma
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis characterized in its full form by severe destructive arthritis, cutaneous nodules, and systemic manifestations.
Karishma D Hemmady+2 more
doaj +1 more source
Bone and soft tissue tumors of hip and pelvis [PDF]
Objective is to identify epidemiologic and radiologic criteria allowing specific diagnoses of tumors and tumor-like lesions in the hip region and pelvis, and to optimize pre-operative staging.Patients with pelvic tumors are usually older, and their ...
Bloem, Johan L., Reidsma, Inge I.
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A RARE CASE OF PULMONARY NON-LANGERHANS CELL HISTIOCYTOSIS [PDF]
Kristen Hughes+3 more
openaire +1 more source
Rare case of Rosai Dorfman disease involving paranasal sinuses in paediatric patient: A case report [PDF]
Rosai Dorfman disease (RDD) is a rare, benign disease of unknown aetiology. It typically presents with massive, painless cervical lymphadenopathy but may have a varied presentation.
Ashish, Gaurav+2 more
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Erdheim Chester disease – 25 year history with early CNS involvement [PDF]
We report a case of Erdheim-Chester disease (ECD) with a 25-year history following initial presentation with diabetes insipidus and brainstem involvement.
Cohen, N+5 more
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Juvenile Xanthogranuloma: Case Report and Literature Review
Sadegh Vahabi-Amlashi, Masoumeh Hoseininezhad, Zahra Tafazzoli Cutaneous Leishmaniasis Research Center, Mashhad University of Medical Sciences, Mashhad, IranCorrespondence: Zahra TafazzoliDepartment of Dermatology, Imam Reza Hospital, Ibn e Sina Street ...
Vahabi-Amlashi S+2 more
doaj
Rosai-Dorfman disease (RDD), or sinus histiocytosis with massive lymphadenopathy, is a rare non-Langerhans cell histiocytosis. We report a case of a 69-year-old male with concurrent appendiceal and rectal masses who underwent CT-guided percutaneous ...
Jenna J. Poldemann+2 more
doaj +1 more source
Cranial unifocal langerhans cell histiocytosis in a female child: a difficult case with S-100 and CD1a immunonegativity [PDF]
A 13-years old female child was carried to Dr. Sardjito General Hospital, Yogyakarta by her mother with chiefcomplaint of a mass on her forehead. Since eight months prior to her visiting, she had a mass on her forehead whichbecame larger slowly without ...
Soeripto, J Bras, Hanggoro Tri Rinonce Sagiri Mangunsudirdjo
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Case series of volar juvenile xanthogranuloma: Clinical observation of a peripheral rim of hyperkeratosis [PDF]
Juvenile xanthogranuloma is a benign histiocytic tumor predominantly occurring in children as yellowish papules on the head and trunk. Presentations on the volar surfaces are rare and may cause diagnostic confusion with pyogenic granuloma, eccrine poroma
Amadi, Ugochukwu+7 more
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