Results 71 to 80 of about 5,398 (224)
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
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
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
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
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
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
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
Toxoplasma IgG Expressed in a Patient With Rosai-Dorfman Disease
Kaohsiung 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
, 2012 Melanoma is a relatively common neoplasm which is increasing in incidence. Melanoma appears as a variegated irregular maculopapular lesion usually on the skin, but possibly on mucosae, conjunctiva, orbit, nails and oesophagus. They may be black, brown,
Magri, Stephanie, Pace, Keith
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