Emperipolesis in a Case of Adult T Cell Lymphoblastic Lymphoma (Mediastinal type)-Detected at FNAC and Imprint Cytology [PDF]
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 +1 more source
ALK-Positive Histiocytosis With Unilateral Breast Involvement: A Case Report. [PDF]
ABSTRACT APH is a rare disorder characterized by the proliferation of ALK‐expressing histiocytes with variable anatomical involvement; however, mammary involvement is exceptionally rare. A 32‐year‐old woman presented with a painless right breast mass. Ultrasound identified a 9 × 8 mm hypoechoic nodule, categorized as BI‐RADS 4A.
Liu X, Ren D, Liang Y.
europepmc +2 more sources
Rosai-Dorfman Disease, Presenting as a Mass in the Trachea: A Case Report. [PDF]
We present a rare case of Rosai–Dorfman disease (RDD) confined solely to the trachea. After initial bronchoscopic resection, systemic corticosteroid therapy was initiated due to lesion progression, successfully stabilizing the disease for 4 years. ABSTRACT A 45‐year‐old woman was referred to our clinic for evaluation of a 17 mm tracheal mass detected ...
Youn T, Lee B, Han J, Jeong BH.
europepmc +2 more sources
The Clinicopathologic Spectrum of Rosai-Dorfman-Destombes Disease in Adults: An Analysis of 16 Cases. [PDF]
ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Trinder M +8 more
europepmc +2 more sources
Rosai–Dorfman disease (RDD) is a rare disorder characterized by the proliferation of histiocytes in lymph nodes. It can occur anywhere in the body but commonly involves the cervical area of the neck.
Erinie Mekheal +6 more
doaj +1 more source
Prednisone and Vincristine for the Treatment of Pediatric Rosai-Dorfman Disease: A Case Report. [PDF]
Purpose Pediatric Rosai–Dorfman disease (RDD) is extremely rare, and the current treatment plan is not unified. We hope that our study provides new ideas for the clinical treatment of RDD. Methods We report a case in which RDD was successfully treated with prednisone and vincristine, resulting in regression of enlarged lymph nodes.
Dun J, Hu Q, Liu A, Wang Y, Zhang A.
europepmc +2 more sources
Rosai-Dorfman Disease With Pure and Multifocal Cutaneous Lesions: A Case Report
A 52‐year‐old woman developed progressive infiltrated purple and hyperpigmented cutaneous lesions in the face, thighs, armpits, chest, and abdomen evolving forone year.
Donia Chebbi +5 more
doaj +1 more source
Megakaryocyte emperipolesis: a new frontier in cell-in-cell interaction
Histology of bone marrow routinely identifies megakaryocytes that enclose neutrophils and other hematopoietic cells, a phenomenon termed emperipolesis.
Pierre Cunin, Peter A. Nigrovic
doaj +1 more source
Occurrence and a possible mechanism of penetration of natural killer cells into k562 target cells during the cytotoxic interaction [PDF]
The cytotoxic interaction between cloned human Natural Killer (NK) cells and K562 target cells was studied using confocal laser scanning microscopy (CLSM) and conventional fluorescence microscopy.
de Grooth, B.G. +6 more
core +3 more sources
Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
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

