Results 81 to 90 of about 6,796 (202)

Acute severe hepatitis and hemophagocytosis in adult onset Still’s disease

, 2015
We report a 44-year-old male Turkish patient with adult onset Still's disease (AOSD) complicated by acute severe hepatitis and hemophagocytosis.
Kara, Elif, Gulluoglu, Mine, Besisik, Fatih, Akyuz, Filiz, Sahutoglu, Tuncay, Dogan, Ibrahim Oner   +5 more
core  

Correlation of AST and number of sinusoidal hemophagocytosis foci; observed at 20x on liver biopsy (Spearman’s Rho r = 0.773, p = 0.015).

, 2019
Correlation of AST and number of sinusoidal hemophagocytosis foci; observed at 20x on liver biopsy (Spearman’s Rho r = 0.773, p = 0.015).
Jacqueline De Gottardi (8201541), Alicia Rovo (121163), Anne Angelillo-Scherrer (591364), Matteo Montani (8201544), Annalisa Berzigotti (387331)   +4 more
core   +1 more source

Diagnostic Dilemma of Disseminated Histoplasmosis Mimicking Hemophagocytosis Lymphohistiocytosis in Patient with Rheumatoid Arthritis on Anti-TNF Therapy: Case Report and Review of the Literature [PDF]

, 2019
Tumor necrosis factor inhibitors (TNFi) have become the cornerstone for the treatment of rheumatoid arthritis and other systemic autoimmune conditions.
Aleksander Lenert, Saurav Suman, Lenert, Aleksander, Suman, Saurav   +3 more
core   +1 more source

Borderline lepromatous leprosy: A case report

Asian Pacific Journal of Tropical Medicine
Rationale: Lepromatous leprosy can have many atypical presentations, obscuring early diagnosis. We present a case of lepromatous leprosy, presenting with atypical features, which made a diagnostic dilemma.
Nilshan Fernando, Chiranthi Welhenge, Ranjan Premaratna, Ahamed Uwyse   +3 more
doaj   +1 more source

Hemophagocytosis: The cause of anemia and thrombocytopenia in congenital syphilis

, 2009
Congenital syphilis is a rare, serious disease that continues to be a major health-care problem. The infected neonate may be asymptomatic or multiple-organ system involvement may occur.
Yarali, Neşe, Akyürek, Nesibe, Zorlu, Pelin, Balaban, Ismail, Uçar, Şit   +4 more
core   +1 more source

Failure of interferon gamma to induce the anti-inflammatory interleukin 18 binding protein in familial hemophagocytosis [PDF]

, 2010
Background: Familial hemophagocytosis (FHL) is a rare disease associated with defects in proteins involved in CD8+ T-cell cytotoxicity. Hyperactivation of immune cells results in a perilous, Th1-driven cytokine storm. We set out to explore the regulation
Nold Marcel F., Claudia A Nold-Petry, Jarisch Andrea, Muhl Heiko, Jarisch, Andrea, Lehrnbecher Thomas, Nold-Petry, Claudia A., Nold, Marcel Friedrich, Andrea Jarisch, Lehrnbecher, Thomas, Pfeilschifter, Josef (Prof. Dr.), Heiko Muhl, Dirk Schwabe, Josef M Pfeilschifter, Pfeilschifter Josef M., Thomas Lehrnbecher, Schwabe Dirk, Nold-Petry Claudia A., Mühl, Heiko, Schwabe, Dirk, Marcel F Nold   +20 more
core   +2 more sources

Linfohistiocitosis hemofagocítica, el espectro desde la enfermedad genética al síndrome de activación macrofágica Hemophagocityc Lymphohistiocytosis: A Spectrum from the Genetic Disorder to the Macrophage Activation Syndrome

Acta Médica Costarricense, 2011
El compromiso de la regulación de la inflamación produce activación excesiva y expansión de macrófagos y linfocitos T que desencadenan una reacción inflamatoria severa, sin vías naturales de control.
Oscar Porras
doaj  

Aggressive natural killer cell leukemia: a case report

International Medical Case Reports Journal, 2017
Ying Hu, Jingbo Wang Department of Hematology, Aerospace Center Hospital, Beijing, People’s Republic of China Abstract: Aggressive natural killer (NK) cell leukemia is a rare hematological malignancy. It often presents with a rapidly declining
Hu Y, Wang J
doaj  

Abstracts of 14th International Symposium on Hodgkin Lymphoma

HemaSphere, Volume 10, Issue S2, October 2026.
wiley   +1 more source

Hemophagocytosis by leukemic megakaryoblasts in acute myeloid leukemia (megakaryoblastic) with t(1;22)(p13;q13);RBM15-MKL1

, 2012
Acute megakaryoblastic leukemia is a rare variant of acute myeloid leukemia, whereby leukemic blasts display characteristic morphologic and phenotypic features indicating megakaryocytoid differentiation. A distinct entity characterized by the t(1;22)(p13;
Bonney, Denise K, Wynn, Robert F, Wiseman, Daniel H; id_orcid   +2 more
core   +1 more source