Results 81 to 90 of about 287,512 (253)
Clinical Case Reports, Volume 13, Issue 8, August 2025.ABSTRACT Brodie's abscess, a subacute form of osteomyelitis, is characterized by localized symptoms and can be challenging to diagnose due to its nonspecific clinical presentation. We report a rare case of distal femoral Brodie's abscess in a healthy child, emphasizing the diagnostic intricacies and management.
Adeel Ahmed Siddiqui +6 more
wiley +1 more source
Терапевтический 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
Primary oral manifestation of Langerhans cell histiocytosis refractory to conventional therapy but susceptible to BRAF-specific treatment: a case report and review of the literature [PDF]
, 2019 Langerhans cell histiocytosis (LCH) is a diagnostic and therapeutic challenge. We report on a rare case of its primary oral manifestation that was treated successfully with the BRAF-specific agent, vemurafenib, after insufficient standard LCH treatment ...
Beck-Broichsitter, Benedicta +8 more
core +1 more source
Rosai-Dorfman Disease: Self-Resolving Unilateral Lymphadenopathy and a Brief Review of Literature
Case Reports in Oncological Medicine, 2018 Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a disease of histiocytic proliferation with no known pathogenesis.
Joshua Feriante, Richard T. Lee
doaj +1 more source
Ovarian endometroid adenocarcinoma in pregnancy [PDF]
, 2011 Background. Ovarian cancer is very rare in pregnancy. It is mainly of epithelial origin, low grade and low malignant potential. Case report. We presented a patient in which ultrasound confirmed the presence of clearly limited tumor in the left ovary when
Dimitrijević Aleksandra +5 more
core +1 more source
Bengal 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
Case Reports in Neurological Medicine, 2017 Polyostotic sclerosing histiocytosis, also known as Erdheim-Chester disease (ECD), is a rare form of non-Langerhans histiocytosis. ECD has wide clinical spectrums which mainly affect skeletal, neurological, dermatological, retroperitoneal, cardiac, and ...
Roaa Ridha Amer +2 more
doaj +1 more source
Langerhans cell histiocytosis of the sphenoid sinus: a case report
The 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
Journal of Gastrointestinal Cancer, 2012 Sinus histiocytosis with massive lymphadenopathy (SHML) was first described in 1969 by Rosai and Dorfman [1]. It is a rare inflammatory disorder with key clinicopathological characteristics such as emperipolesis and positive immunostaining for S-100 ...
Minerva A. Romero Arenas +3 more
semanticscholar +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 +5 more
doaj +1 more source