Results 1 to 10 of about 3,473 (178)

Florid dermatopathic lymphadenopathy—A morphological mimic of Langerhans cell histiocytosis

Clinical 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, Gaurav Goyal, Jarrett J. Failing, Ronald S. Go, Karen L. Rech   +4 more
doaj   +1 more source

Rosai and Dorfman Disease with Pleural Involvement: Case Report

The 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, Sonia Toujani, Nadia Mehiri, Bechir Louzir, Nidham Kchir, Majed Beji   +5 more
doaj   +1 more source

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): a case report and review of Literature

Journal of Health Science and Medical Research (JHSMR), 2003
Sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease is an unusual, benign, selflimited condition of unknown etiology which generally presents as massive bilateral cervical lymphadenopathy in children.
R Tangsathitporn, A Nitiruangjarus
doaj  

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

Iraqi 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

Diagnosis of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) by fine needle aspiration cytology

Journal of Cytology, 2009
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.
Kushwaha Rashmi, Ahluwalia Charanjeet, Sipayya Varuna   +2 more
doaj  

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

Journal of Cytology, 2011
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala, Asha Agarwal, Sanjay Kala   +2 more
doaj   +1 more source

Sinus Histiocytosis

, 2006
The author describes a case of massive lynphadenopathy, fever, astenia and sweating, with 3 weeks evolution. The patient was investigated in a health unit in Sapiranga – RS, Brazil, where he diagnosed with sinus histiocytosis (Rosai-Dorfman disease). After initial treatment in the health unit, the patient was transferred to a reference service.
openaire   +1 more source

Rosai–Dorfman disease as chronic bilateral granulomatous anterior uveitis: A case report

SAGE Open Medical Case Reports
Rosai–Dorfman disease is a rare non-Langerhans cell histiocytosis disorder, also known as sinus histiocytosis, with massive lymphadenopathy. Rosai–Dorfman disease is classified into nodal and extranodal diseases.
Yaninsiri Ngathaweesuk, Chaisiri Jumroendararasame   +1 more
doaj   +1 more source

Unusual Neurological Manifestation of Langerhans Cell Histiocytosis in an Adult

Ear, Nose & Throat Journal
Langerhans Cell Histiocytosis is a rare disorder characterized by an abnormal proliferation of Langerhans cells in one or multiple organs. It rarely presents with a central vestibular involvement.
Imen Achour MD, Ines Kharrat MD, Youssef Hbaieb MD, Mariam Ben Ayed MD, Malek Mnejja MD, Bouthaina Hammami MD, Basma Souissi MD, Ilhem Charfeddine MD   +7 more
doaj   +1 more source

Langerhans cell histiocytosis in sphenoid sinus with vision impairment: Case report and literature review

Science Progress
Langerhans cell histiocytosis (LCH) is a neoplastic disease characterized by aberrant proliferation of the mononuclear phagocyte system, predominantly affecting children under the age of 3 years.
Min-Shan Li, Xing-Liang Wu, Ao Huang, Heng Wang   +3 more
doaj   +1 more source