Results 71 to 80 of about 283,013 (233)

Skull Base Langerhans Cell Histiocytosis with Diabetes Insipidus and Panhypopituitarism- A Rare Clinical Entity

open access: yesBengal Journal of Otolaryngology and Head Neck Surgery, 2017
Introduction A case of Langerhans cell histiocytosis (LGH) involving extensive area of base of skull resulting in panhypopituitarism and diabetes insipidus (DI) is reported.
Anirban Ghosh   +2 more
doaj   +3 more sources

Intraosseous Rosai-Dorfman disease diagnosed by touch imprint cytology evaluation: A case series [PDF]

open access: yes, 2018
Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease (RDD) is a rare benign disorder that primarily affects the lymph nodes. Localized lymphadenopathy is the most common clinical manifestation of this disorder.
Alvarez Alegret   +29 more
core   +2 more sources

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 Histiocytosis with Massive Lymphadenopathy: A Case Report with Pleural Effusion and Cervical Lymphadenopathy [PDF]

open access: yes, 2009
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare disorder characterized by a nonneoplastic proliferation of distinctive histiocyte cells within lymph node sinuses and lymphatics in extranodal sites. SHML occurs worldwide and is primarily
Ahsan   +25 more
core   +2 more sources

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

Solitary fibrous tumour of the nose and nasopharynx [PDF]

open access: yes, 1993
A case of solitary fibrous tumour of the nasal cavity is reported. These tumours, rare in the nose, are believed to be similar to fibrous mesotheliomas of the pleural cavity.
DeGaetano, James   +2 more
core  

Sinus histiocytosis with lymphadenopathy - a case report

open access: yesKYAMC Journal, 2013
Sinus histiocytosis with lymphadenopathy is a rare condition of unknown etiology that is characterized by the overproduction of histiocytes accumulating in the lymph node sinuses and in the lymphatics of extranodal sites if involved. Lymph nodes of the neck are the most common place of histiocyte accumulation, although other lymph nodes and organs may ...
Md. Zulfikar Ali   +2 more
openaire   +2 more sources

Langerhans cell histiocytosis of the sphenoid sinus: a case report

open access: yesThe Turkish Journal of Pediatrics, 2010
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare disorder characterized by clonal proliferation and excess accumulation of pathologic Langerhans cells causing local or systemic effects.
Guohua Yu   +5 more
doaj  

Extra-osseous involvement of Langerhans' cell histiocytosis in children [PDF]

open access: yes, 2018
The predominant clinical and radiological features of Langerhans' cell histiocytosis (LCH) in children are due to osseous involvement. Extra-osseous disease is far less common, occurring in association with bone disease or in isolation; nearly all ...
Eich, Georg   +5 more
core  

Ocular involvement in sinus histiocytosis with massive lymphadenopathy. [PDF]

open access: yesBritish Journal of Ophthalmology, 1988
Sinus histiocytosis with massive lymphadenopathy is a distinct clinical entity, with ophthalmic involvement in 10% of patients. Orbital as well as eyelid lesions have been described as part of the extra-lymph node involvement of this disorder. We recently examined a young boy with sinus histiocytosis with a bulbar conjunctival mass and chronic ...
Zeynel A. Karcioglu, B Allam, M S Insler
openaire   +3 more sources

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