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This case report describes the management of a middle-aged woman with abnormal uterine bleeding who developed Anti-Jk and Anti-M antibodies following multiple transfusions, illustrating the challenges in transfusion medicine. Despite initial negative antibody screening, repeat testing post-transfusion revealed these clinically significant antibodies, demonstrating the dynamic nature of alloimmunization. The case highlights the importance of the MNS and Kidd blood group systems in transfusion reactions, particularly the risk of delayed hemolysis with anti-Jk antibodies. Through serial antibody screening, advanced serological techniques, and close blood bank collaboration, antigen-negative blood was successfully provided for her urgent surgical needs. This report emphasizes the critical need for vigilant antibody monitoring in multitransfused patients, the value of interdisciplinary coordination, and the importance of ongoing clinician education to improve transfusion safety in complex cases.
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http://dx.doi.org/10.1002/ccr3.70696 | DOI Listing |
J Pathol Transl Med
September 2025
Department of Pathology and Laboratory Medicine, University of California, Irvine (UCI), Irvine, CA, USA.
Chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) is a clinically indolent lymphoproliferative disorder characterized by accumulation of mature B-cell lymphocytes. Given the common CD5 co-expression, mantle cell lymphoma (MCL) is one of the most important entities in the differential diagnosis. MCL and CLL/SLL might exhibit overlapping morphologic and immunohistochemical features, making diagnosis particularly difficult in cases of composite lymphomas.
View Article and Find Full Text PDFMov Disord Clin Pract
September 2025
Department of Neurology, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu, Taiwan.
Br J Dermatol
September 2025
Department of Dermatology, Sainte-Justine University Hospital Center, Montreal, QC, Canada.
Zhong Nan Da Xue Xue Bao Yi Xue Ban
May 2025
Department of Nephropathy and Rheumatology, Third Xiangya Hospital, Central South University, Changsha 410013.
Dent disease is a rare X-linked recessive inherited renal tubular disorder characterized by low molecular weight proteinuria (LMWP), hypercalciuria, nephrocalcinosis, and other clinical features, and can lead to progressive renal failure. It is primarily caused by mutations in the gene. This article reports the case of a 10-year-old male patient of Chinese descent who was incidentally found to have asymptomatic proteinuria during a routine health examination.
View Article and Find Full Text PDFMultimed Man Cardiothorac Surg
September 2025
Kawasaki Aortic Center, Kawasaki Saiwai Hospital, Kawasaki, Japan.
Kommerell's diverticulum (KD) combined with a right-sided aortic arch (RAA) and an aberrant left subclavian artery (ALSA) is a rare congenital vascular anomaly causing significant compressive dysphagia. Treatment options, including open surgery, thoracic endovascular aortic repair and hybrid approaches, are debated due to anatomical complexities. We report a 48-year-old female with dysphagia from symptomatic KD, RAA and ALSA, clearly delineated by preoperative computed tomography angiography.
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