Thoracic, abdominal and musculoskeletal involvement in Erdheim-Chester disease: CT, MR and PET imaging findings. [PDF]
, 2014 BACKGROUND: Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis with characteristic radiological and histological features. This entity is defined by a mononuclear infiltrate consisting of lipid-laden, foamy histiocytes that stain
Antunes, C, Donato, P, Graça, B
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A case of canine cutaneous reactive histiocytosis over the body trunk in an adult pit bull terrier
Veterinary Record Case Reports, Volume 13, Issue 4, December 2025.Abstract The objective of this report is to present a case of canine cutaneous reactive histiocytosis with a high number of dendritic cells. A 7‐year‐old male pit bull terrier was presented with a 5‐month history of skin nodules and plaques on the trunk of varying diameter, along with corneal oedema and anterior uveitis.
Ioanna Papadogiannaki +3 more
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Altano-axial subluxation with torticollis secondary to Langerhans cell histocytosis
Interdisciplinary Neurosurgery, 2017 Langerhans Cell Histiocytosis is a rare disease featuring aberrant proliferation of dendritic cells that can infiltrate the bony skeleton. The authors report a case of six-year-old female presenting with torticollis. She was found to have extensive lytic
Joshua Y. Chua, MD +5 more
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Caso para diagnóstico Case for diagnosis
Anais Brasileiros de Dermatologia, 2011 Relatamos um caso de histiocitose cefálica benigna em uma criança do sexo masculino, de um ano e três meses de idade que desenvolveu múltiplas pápulas na região malar bilateralmente, sem outros comemorativos associados.
Maria de Fátima Guimarães Scotelaro Alves +4 more
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Rare Presentation of a Rare Orthopedic Pathology: Erdheim Chester Disease [PDF]
, 2017 In 1930, William Chester and pathologist Jakob Erdheim discovered the pathology currently known as Erdheim Chester disease. There are only approximately 249 histologically confirmed patients to have been diagnosed with this disease as noted in the ...
Samona J, Owen J, Martin S
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Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage
Dermatologica Sinica, 2015 Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juvenile ...
Hikmet Tekin Nacaroglu +6 more
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Multiple cutaneous reticulohistiocytoma
Indian Journal of Dermatology, 2016 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
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Better a Broader Diagnosis Than a Misdiagnosis: The Study of a Neoplastic Condition in a Male Individual who Died in Early 20th Century (Coimbra, Portugal) [PDF]
, 2013 The paleopathological record of neoplastic conditions in the past is considered scarce. The detection of tumours in ancient populations is hindered by the quality and quantity of signs visible on the skeleton, the methodological approach, the ...
Cunha, Eugénia +2 more
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Juvenile Xanthogranuloma: Case Report and Literature Review
International Medical Case Reports Journal, 2020 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
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