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Indian J Dermatol
April 2024
From the Department of Dermatology, Venereology and Leprology, Government Medical College and Hospital, Chandigarh, Punjab, India.
Clin Exp Rheumatol
December 2022
Pathophysiology Department, Athens School of Medicine, National and Kapodistrian University of Athens, Greece.
Objectives: Primary Sjögren's syndrome (pSS) is a systemic autoimmune disease characterised by oral and eye dryness. A minority of patients can present without dryness but studies on their clinico-laboratory manifestations are scarce. Our purpose was to describe the clinical phenotype of pSS patients lacking sicca symptoms.
View Article and Find Full Text PDFMedicine (Baltimore)
August 2022
Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Korea.
No study has evaluated the effect of therapeutic granulocyte colony-stimulating factor (G-CSF) in preventing recurrence of febrile neutropenia (FN) and survival outcomes in gynecologic cancer patients. Objective of this study is to optimize and to identify the use of G-CSF and identify the critical factors for preventing the recurrence of FN in women undergoing chemotherapy for the treatment of gynecologic cancer. The medical records of consecutive patients who underwent chemotherapy for the treatment of gynecologic cancer and experienced FN at least once were retrospectively reviewed.
View Article and Find Full Text PDFMycoses
October 2022
Indonesian Dermatomycosis Study Group-Indonesian Society of Dermatology and Venereology, Jakarta, Indonesia.
Pan Afr Med J
January 2021
Microbiology and Immunology Department, Faculty of Medicine, Zagazig University, Sharkia, Egypt.
Introduction: hemophagocytic lymphohistiocytosis (HLH) is an immunological disease characterized by hemophagocytosis of blood cells and proliferation of T-cells and histiocytes in the spleen and bone marrow then infiltration into body organs. Familial HLH (FHL) is a fatal disorder and determining gene mutations is a good guide for predicting the prognosis and choosing treatment options. This study aimed to illustrate the clinical, laboratory characteristics, including perforin gene mutation screening, treatment and survival outcome of pediatric HLH patients.
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