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
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Wegener's granulomatosis (WG) could be a lethal disease if not diagnosed and managed timely. Oral involvement is rare and often presents as gingival hyperplasia with a traditional “strawberry gingivitis” appearance. Dental practitioners may be the first ones to encounter WG and may be able to prevent disease progression like the present case ...
Samaneh Salari +4 more
wiley +1 more source
Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature
Journal of the Belgian Society of Radiology, 2014 Rosai-Dorman disease (RDD) is a rare disorder of proliferative histiocytes with an unknown etiology. It is also known as sinus histiocytosis with massive lymphadenopathy. Most patients present with painless cervical lymphadenopathy due to accumulation of
H M Duijsens +4 more
doaj +1 more source
Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]
National Journal of Laboratory Medicine, 2018 Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan +4 more
doaj +1 more source
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
Primary intraosseous meningioma: an osteosclerotic bone tumour mimicking malignancy [PDF]
, 2016 BACKGROUND: Sclerotic tumours of the calvarial bones are rare and may be due to primary and secondary bone tumours as well as extradural tumours of meningeal origin. CASE PRESENTATION: We report a case of primary intraosseous meningioma (PIM) which arose
M. Vlychou +3 more
core +1 more source
Thoracotomies in Children in Low to Middle Income Countries: The Indications for Surgery
Pediatric Pulmonology, Volume 60, Issue 10, October 2025.ABSTRACT Introduction There is a scarcity of data on the utilization of thoracotomy for lung pathology in children in low‐ and middle‐income countries (LMICs). These countries have high burdens of infectious diseases, especially tuberculosis, hydatic disease and Human immunodeficiency virus (HIV).
Jacobus Botha +10 more
wiley +1 more source
Childhood Cancer Survivors in Latin America: Insights Into Health Outcomes and Information Needs
Pediatric Blood &Cancer, Volume 72, Issue 9, September 2025.ABSTRACT Background Childhood cancer survivors (CCSs) face long‐term health challenges, yet the health and specific needs of Latin American survivors remain underexplored. This study aimed to describe the health‐related, psychosocial late effects, and information needs among CCSs in the region. Methods This mixed‐method study combined quantitative data
Ana Carolina Izurieta‐Pacheco +17 more
wiley +1 more source
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
Rosai-Dorfman Disease- A Surprise diagnosis in Follow up of SCC Pyriform Sinus -Post Surgery and CTRT [PDF]
National 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