Results 31 to 40 of about 1,903 (165)
Purely cutaneous rosai-dorfman disease with immunohistochemistry
Indian Journal of Dermatology, 2013 Background: The cutaneous form of Rosai-Dorfman disease (RDD) is a rare entity that manifests solely with skin papules or nodules and does not present with the usual myriad of symptoms of classical RDD.
Uzma Farooq +3 more
doaj +1 more source
Histopathology, EarlyView.New concepts, innovations and some issues have emerged since the adoption a decade ago of WHO/ISUP grading for CCRCC and PRCC. Continued use of the WHO/ISUP grading for CCRCC and PRCC has been upheld by newer studies, and practice guidance for some of the grading issues, where data are available, is provided.
Gladell P. Paner +4 more
wiley +1 more source
Journal of Cytology, 2009 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
Megakaryocyte emperipolesis in a child with chronic neutropenia: an unusual coexistence
The Turkish Journal of Pediatrics, 2001 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 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
A rare case of purely cutaneous Rosai–Dorfman’s disease: Xanthoma-like presentation
Indian Journal of Dermatopathology and Diagnostic Dermatology, 2022 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
Online Journal of Health & Allied Sciences, 2011 Emperipolesis is a condition in which viable hematopoetic cells are seen intact in the cytoplasm of host cell without damage. This phenomenon is seen in many physiologic and pathologic conditions, its presence in Rosai Dorfman disease (RDD) is ...
Amita K +3 more
doaj
Rosai-Dorfman Disease: A Clinico-pathological Presentation of Three Cases and Review of Literature [PDF]
Journal of Clinical and Diagnostic Research, 2018 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
Striking emperipolesis in megakaryocytes of gray platelet syndrome [PDF]
Blood, 2019 ![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