Results 61 to 70 of about 110,080 (174)

Toxoplasma IgG Expressed in a Patient With Rosai-Dorfman Disease

open access: yesKaohsiung Journal of Medical Sciences, 2010
Rosai-Dorfman Disease (RDD) is a rare benign disease characterized by sinus histiocytosis with massive lymphadenopathy. RDD can be differentiated from other types of histiocytosis by immunochemical analysis, as RDD is positive for S100.
Hung-Ju Liao, Ching-Wen Chiang
doaj   +1 more source

Florid dermatopathic lymphadenopathy—A morphological mimic of Langerhans cell histiocytosis

open access: yesClinical Case Reports, 2018
Key Clinical Message The histopathology of reactive florid dermatopathic lymphadenopathy shows overlap with Langerhans cell histiocytosis (LCH) involving the lymph node, which may lead to misdiagnosis.
Aishwarya Ravindran   +4 more
doaj   +1 more source

Metachronous Primary Pancreatic Neuroendocrine Tumor and Adenocarcinoma: A Case Report

open access: yesCancer Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Background Pancreatic ductal adenocarcinoma (PDAC) has a dismal prognosis, with most patients presenting with advanced disease. Surgical resection remains the only potentially curative option, yet recurrence rates are high. Case We present a rare case of metachronous primary pancreatic neuroendocrine tumor (PanNET) and PDAC in a 71‐year‐old ...
Anastasia S. Fatyanova   +7 more
wiley   +1 more source

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

open access: yes, 2003
Rosai-Dorfman disease is a rare benign idiopatic histiocytic proliferative disorder. It is also known as sinus histiocytosis with massive lymphadenopathy.
Erkan Özüdoğru   +4 more
core  

Giant coronary sinus aneurysm and multiple coronary artery aneurysms in a pediatric patient [PDF]

open access: yes, 2015
Giant coronary sinus aneurysm is extremely rare in pediatric population. It was first reported in 1983 by Ho SY et al. Cerebrovascular accident, shock, myocarditis and severe myocardial dysfunction requiring extracorporeal membrane oxygenation are also
Abbas, Ume L.   +2 more
core  

Rosai and Dorfman Disease with Pleural Involvement: Case Report

open access: yesThe Scientific World Journal, 2008
Sinus histiocytosis with massive lymphadenopathy (SHLM) disease is considered to be an indolent and self-limiting pathology. However, severe morbidity and mortality have been attributed to complications of SHLM.
Jouda Cherif   +5 more
doaj   +1 more source

Association of sinus histiocytosis with massive lymphadenopathy and idiopathic hypereosinophilic syndrome [PDF]

open access: yes, 1987
A patient was evaluated because of edema, pruritus and generalized painless lymphadenopathy. Laboratory tests showed marked eosinophilia without known etiology. CT scan of abdomen revealed multiple lymph nodes in retroperitoneal area.
Wunaii, Herman   +5 more
core  

Management of a patient with Rosai–Dorfman syndrome and large adrenal pheochromocytoma

open access: yesIraqi Journal of Hematology, 2018
Sinus histiocytosis with massive lymphadenopathy that known as Rosai Dorfman syndrome (RDS)is a rare histiocytic disease which includes benign lymph nodes (LN) enlargement with extra-lymphatic soft tissue involvement.
Taha O Mahwi, Najmaddin Khoshnaw
doaj   +1 more source

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

open access: yes, 2012
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.
Gbotolorun, OM   +4 more
core   +1 more source

Langerhans cell histiocytosis of maxillary sinus

open access: yes, 2012
Langerhan cell histiocytosis is a rare disease and usually occurs in paediatric age group. This disease may involve single or multiple organs system and has an unpredictable course of disease.
Tuan Norhafizah binti Tuan Zakaria
core  

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