Veterinary Record Case Reports, EarlyView.Abstract This report describes a case of refractory ionised hypercalcaemia, of 12 months duration, in an 11‐year‐old, male, neutered beagle diagnosed with metastatic histiocytic sarcoma at postmortem examination. In this case, the parathyroid hormone levels were at the lower end of the reference interval, the parathyroid hormone‐related peptide was ...
Kerry E. Rolph +5 more
wiley +1 more source
An unusual Erdheim-Chester disease with orbital involvement: A case report [PDF]
, 2016 Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Bencivinni, F. +5 more
core +2 more sources
Aggressive Neoplasms That Mimic Chronic Endodontic Lesions: A Multi‐Institutional Case Series
Australian Endodontic Journal, EarlyView.ABSTRACT This study aimed to report sociodemographic, clinicopathologic and radiological features of 12 cases of aggressive neoplasms that were clinically diagnosed as chronic endodontic lesions. The series comprised seven females (58.33%) and five males (41.67%), with a mean age of 48.9 ± 19.19 years (range: 16–75 years).
Natália Gonçalves Macedo +11 more
wiley +1 more source
Differential Diagnoses of Systemic Mastocytosis in Routinely Processed Bone Marrow Biopsy Specimens: A Review [PDF]
, 2010 Diagnosis of systemic mastocytosis (SM) is mainly based on the morphological demonstration of compact mast cell infiltrates in various tissue sites. In almost all patients such infiltrates are detected in the bone marrow.
Horny, H. -P., Sotlar, K., Valent, P.
core +1 more source
Steroid‐responsive generalised sterile necrotising pyogranulomatous lymphadenitis in a cat
Journal of Small Animal Practice, EarlyView.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
Histiocytosis in Nigerian children: A report of two variants
Nigerian Journal of Paediatrics, 2021 Histiocytoses are a rare group of proliferative disorders with very similar clinical and histological pictures. We present a case report of two variants seen in an eight month old female and five month old male in a tertiary hospital in southern Nigeria.
Udo E +3 more
doaj
Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
South African Journal of Radiology, 2023 Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented.
Smily Sharma +3 more
doaj +1 more source
Nuclear grade and sinus histiocytosis in cancer of the breast [PDF]
Cancer, 1969 The survival of a uniform series of 318 cases of Columbia Clinical Classification stage A breast carcinoma for 10 or more years postmastectomy was analyzed, with particular reference to influence of the nuclear grade of the cancer and sinus histiocytosis of the axillary lymph nodes.
Gilbert H. Friedell +5 more
openaire +3 more sources
Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report
Anais Brasileiros de Dermatologia, 2010 A doença de Rosai-Dorfman, também denominada histiocitose sinusal com linfadenopatia maciça, é histiocitose de células não Langerhans, idiopática e de curso benigno.
Josie da Costa Eiras +4 more
doaj +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