Results 51 to 60 of about 2,806 (197)
Drug-induced liver injury [PDF]
Drug-induced liver injury (DILI) remains the most common cause of acute liver failure (ALF) in the western world. Excluding paractamol overdose, nearly all DILI encountered in the clinical setting is idiosyncratic in nature, since affected individuals ...
A +12 more
core +1 more source
This study examines variation of morphologic features, including emperipolesis, during the evolution of a case of Rosai Dorfman Disease (RDD). A 44-year-old male patient with RDD affecting the salivary glands, cervical lymph nodes, nasal and maxillary ...
Iyer Venkateswaran +2 more
doaj
Rosai-Dorfman Disease- A Surprise diagnosis in Follow up of SCC Pyriform Sinus -Post Surgery and CTRT [PDF]
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
A rare case of purely cutaneous Rosai–Dorfman’s disease: Xanthoma-like presentation
Rosai–Dorfman’s disease (RDD) is sinus histiocytosis with massive lymphadenopathy. Cutaneous RDD is a rare entity that presents with isolated skin involvement without any systemic involvement. We report a 35-year-old man with an asymptomatic large nodule
Sushanti Jadhav +3 more
doaj +1 more source
Megakaryocyte emperipolesis in a child with chronic neutropenia: an unusual coexistence
The term emperipolesis defines the temporary presence of one cell within another's cytoplasm. In clinical use, megakaryocyte emperipolesis is the penetration of hematopoietic cells into the cytoplasm of megakaryocytes.
D Aslan, S Yetgin
doaj
Rosai-Dorfman Disease: A Clinico-pathological Presentation of Three Cases and Review of Literature [PDF]
Rosai-Dorfman Disease (RDD) or Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is a rare histiocytic disorder of unknown aetiology which presents as a benign, self-limiting disease of phagocytic histiocytes occurring mainly in the first and ...
Francis Ikechukwu Ukekwe +4 more
doaj +1 more source
Defective neutrophil clearance in JAK2V617F myeloproliferative neoplasms drives myelofibrosis via immune checkpoint CD24. [PDF]
Myeloproliferative neoplasms (MPNs) are hematopoietic stem cell-driven malignancies marked by excessive myelopoiesis and high risk of myelofibrosis, which remains therapeutically challenging. Senescent neutrophils home daily to the bone marrow (BM) to be
Khatib-Massalha E +15 more
europepmc +3 more sources
Striking emperipolesis in megakaryocytes of gray platelet syndrome [PDF]
![Figure][1] An 11-year-old girl was diagnosed with gray platelet syndrome (GPS) with compound heterozygous NBEAL2 mutations after presenting with recurrent epistaxis and thrombocytopenia. Bone marrow examination was performed to evaluate for myelofibrosis.
Eric McGinnis, Kate M. Chipperfield
openaire +2 more sources
Hyperammonemia-induced toxicity for the developing central nervous system [PDF]
In pediatric patients, hyperammonemia can be caused by various acquired or inherited disorders such as urea cycle deficiencies or organic acidemias. The brain is much more susceptible to the deleterious effects of ammonium during development than in ...
Braissant, O., Cagnon, L.
core +1 more source
Abstract Objectives To assess whether the prognosis of pediatric‐onset inflammatory bowel disease (IBD) is influenced by its association with primary sclerosing cholangitis (PSC) considering medical treatment, bowel resection, risk of cancer, and mortality. Methods A retrospective population‐based study was conducted using data from the EPIMAD Registry,
Marie‐Laura Godet +10 more
wiley +1 more source

