Results 81 to 90 of about 289,368 (261)
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
Pediatric Allergy and Immunology, Volume 37, Issue 1, January 2026.
Clément Triaille +2 more
wiley +1 more source
The Clinical Respiratory Journal, Volume 19, Issue 9, September 2025.We discuss a case where an innovative combination of photodynamic therapy (PDT) and local radiation therapy to address the diagnostic and therapeutic challenges associated with PPSS resulted in significant improvements in clinical symptoms and patient survival, demonstrating the success of this treatment.
Ran An +5 more
wiley +1 more source
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
Steroid‐responsive generalised sterile necrotising pyogranulomatous lymphadenitis in a cat
Journal of Small Animal Practice, Volume 66, Issue 9, Page 670-675, September 2025.A 1.5‐year‐old neutered male cat was presented with fever, inappetence, lethargy and marked generalised lymphadenopathy of 4 days duration. Excisional biopsy of peripheral lymph nodes revealed necrotising pyogranulomatous lymphadenitis. Extensive investigation failed to identify an underlying infectious [bacterial (Bartonella, Mycobacteria, Mycoplasma,
L. Lecot +4 more
wiley +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
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
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
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