Results 71 to 80 of about 289,368 (261)

Rosai-Dorfman Disease- A Surprise diagnosis in Follow up of SCC Pyriform Sinus -Post Surgery and CTRT [PDF]

open access: yesNational Journal of Laboratory Medicine, 2013
Rosai-Dorfman disease also known as Sinus Histiocytosis with massive Lymphadenopathy (SHML). SHML was first described by Rosai and Dorfman in 1969 [1] and is now considered a non malignant inflammatory disorder in which the precise origin of ...
Nandeesh M, Anitha T.K., Santosh R.
doaj   +1 more source

Sinus Histiocytosis with Massive Lymphadenopathy (Rosai-Dorfman Disease): A Case Report and Literature Review

open access: yesInternational Archives of Otorhinolaryngology, 2014
Introduction Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement.
R. Pradhananga   +3 more
semanticscholar   +1 more source

Childhood Cancer Survivors in Latin America: Insights Into Health Outcomes and Information Needs

open access: yesPediatric Blood &Cancer, Volume 72, Issue 9, September 2025.
ABSTRACT Background Childhood cancer survivors (CCSs) face long‐term health challenges, yet the health and specific needs of Latin American survivors remain underexplored. This study aimed to describe the health‐related, psychosocial late effects, and information needs among CCSs in the region. Methods This mixed‐method study combined quantitative data
Ana Carolina Izurieta‐Pacheco   +17 more
wiley   +1 more source

Bagaimana Prognosis Histiocytosis? Sebuah Laporan Kasus [PDF]

open access: yes, 2013
Penderita histiocytosis dengan keterlibatan multiorgan dan disertai gangguan fungsi organ mempunyai prognosis buruk dan tingkat mortalitas tinggi. Dilaporkan seorang penderita histiocytosis, usia 1 tahun 1 bulan yang datang dengan kelainan di kulit ...
Lestari, R. D. (Rini)   +1 more
core  

Primary intraosseous meningioma: an osteosclerotic bone tumour mimicking malignancy [PDF]

open access: yes, 2016
BACKGROUND: Sclerotic tumours of the calvarial bones are rare and may be due to primary and secondary bone tumours as well as extradural tumours of meningeal origin. CASE PRESENTATION: We report a case of primary intraosseous meningioma (PIM) which arose
M. Vlychou   +3 more
core   +1 more source

A case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) in a patient with diffuse large B-cell lymphoma and chronic hepatitis B virus infection

open access: yesТерапевтический архив, 2012
The paper describes a case of diffuse large B-cell lymphoma detected in a patient 13 months after sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease (RDD) being diagnosed together with active hepatitis B virus infection ...
A L Melikian   +3 more
doaj  

Sinus and palatal Rosai-Dorfman Disease: Case report and review of the literature

open access: yesAmerican Journal of Otolaryngology
Rosai-Dorfman Disease (RDD) is a rare non-Langerhans cell histiocytosis. We present a unique case of RDD with sinus and palatal involvement managed with surgical biopsy, debulking and radiation, and review the literature on this topic.
Clare Moffatt   +5 more
doaj   +1 more source

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital

open access: yesNigerian Dental Journal, 2011
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, benign disease of unknown aetiology. This disease typically presents with massive, painless cervical lymphadenopathy but may occur in a wide variety of extranodal sites.
O. F. Ajayi   +4 more
doaj   +1 more source

Case for diagnosis [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2014
Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limited, only involves skin and subcutaneous tissue and typically occurs as histiocyte-rich inflammatory infiltrates, manifesting as erythematous to brown ...
Han Ma   +4 more
doaj   +1 more source

Suspected calcitriol‐mediated hypercalcaemia and postmortem diagnosis of histiocytic sarcoma in a dog

open access: yesVeterinary Record Case Reports, Volume 13, Issue 3, September 2025.
Abstract This report describes a case of refractory ionised hypercalcaemia, of 12 months duration, in an 11‐year‐old, male, neutered beagle diagnosed with metastatic histiocytic sarcoma at postmortem examination. In this case, the parathyroid hormone levels were at the lower end of the reference interval, the parathyroid hormone‐related peptide was ...
Kerry E. Rolph   +5 more
wiley   +1 more source

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