Results 41 to 50 of about 4,878 (159)
Radiology Case Reports, 2021 Rosai–Dorfman disease is a non–Langherans cell histiocytosis typically revealed by a lymphadenopathy. Central nervous system involvement is rare, exceptionally isolated, and usually consists of dural masses mimicking meningioma.
Guillaume Friconnet, MD +7 more
doaj +1 more source
Diagnosis of Rosai-Dorfman Disease by Fine Needle Aspiration Cytology in a Case with Cervical Lymphadenopathy and Nasal Mass [PDF]
, 2011 We report a case of Rosai-Dorfman Disease, a rare non neoplastic proliferative disorder of the cells of macrophage-histiocyte family, in a case with cervical lymphadenopathy and nasal mass diagnosed by fine needle aspiration ...
Jena, M
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Case series of volar juvenile xanthogranuloma: Clinical observation of a peripheral rim of hyperkeratosis [PDF]
, 2014 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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Case Report and Literature Review: Intrathyroid Thymic Carcinoma
Journal of Clinical Ultrasound, Volume 54, Issue 2, Page 461-464, February 2026.This case report highlights the challenges in diagnosing intrathyroid thymic carcinoma (ITTC), a rare thyroid tumor, and underscores the importance of postoperative pathology for confirmation. The study emphasizes the good prognosis of ITTC with appropriate surgical management.
Jia‐Yue Sun +3 more
wiley +1 more source
Rosai-Dorfman disease with pulmonary involvement mimicking bronchogenic carcinoma
Journal of Cardiothoracic Surgery, 2020 Background Rosai-Dorfman disease is a histiocytic lesion that affects lung rarely. Case presentation We present a 52-year-old female diagnosed with right intrabronchial mass invading the bronchial wall and the extrabronchial tissues with lymphadenopathy.
Haneen Al-Maghrabi +4 more
doaj +1 more source
, 2018 Rosai-Dorfman disease is a rare, usually benign, entity that mostly affects children and adolescents. We report a clinical case in which the most common clinical and imaging manifestation is present: cervical lymphadenopathy. Histological confirmation is
Carvalho, André +5 more
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International Journal of Laboratory Hematology, Volume 48, Issue 1, Page 12-25, February 2026.ABSTRACT Monocytes are key components of the Mononuclear Phagocyte System, crucial in immune defense, inflammation, and tissue repair. Accurate identification and classification of monocyte lineage cells are essential for diagnosing both reactive and clonal hematologic disorders.
Gina Zini +10 more
wiley +1 more source
BMC Ophthalmology, 2019 Background Rosai-Dorfman disease is a rare non–Langerhans cell histiocytosis. Ocular involvement is even rarer, mostly involving the orbit and eyelids, although marginal corneal ulcers, uveitis, and epibulbar masses have also been reported, and is ...
Yu-Kuei Lee +3 more
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Le syndrome de rosai dorfman de l’enfant (a propos d’un cas) [PDF]
, 2015 Le syndrome de rOSaï DOrFman ou histiocytose sinusale avec lymphadénopathie massive est une maladie rare d’étiologie inconnue, peut se voir à tout âge, l’enfant n’étant pas épargné.
Belaabida, B +4 more
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ALK‐Positive Histiocytosis With Unilateral Breast Involvement: A Case Report
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT APH is a rare disorder characterized by the proliferation of ALK‐expressing histiocytes with variable anatomical involvement; however, mammary involvement is exceptionally rare. A 32‐year‐old woman presented with a painless right breast mass. Ultrasound identified a 9 × 8 mm hypoechoic nodule, categorized as BI‐RADS 4A.
Xuechun Liu, Dong Ren, Yanfang Liang
wiley +1 more source