Revista do Colégio Brasileiro de CirurgiõesOBJETIVOS: Para se evitar o estado asplênico, muitas medidas preservadoras do baço têm sido propostas na literatura, como a esplenorrafia, a esplenectomia parcial com preservação dos vasos hilares e o auto-implante de tecido esplênico.
Rodrigo Gomes da Silva +4 more
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BACTERIAL INFECTIONS FOLLOWING SPLENECTOMY FOR MALIGNANT AND NONMALIGNANT HEMATOLOGIC DISEASES
Mediterranean Journal of Hematology and Infectious Diseases, 2015 Splenectomy, while often necessary in otherwise healthy patients after major trauma, find its primary indication for patients with an underlying malignant or nonmalignant hematologic diseases.
Giuseppe Leone, Eligio Pizzigallo
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Quality of life and behavioral functioning in Dutch pediatric patients with hereditary spherocytosis [PDF]
, 2014 The objective of this study was to evaluate health-related quality of life (HRQoL) and behavioral functioning in pediatric patients with hereditary spherocytosis (HS).
Bronner, M.B. (Madelon) +5 more
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From Hemolysis to Lupus: A Case of Evans Syndrome Revealing Systemic Autoimmunity
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT Evans syndrome (ES), the coexistence of autoimmune hemolytic anemia and immune thrombocytopenia, can unmask systemic autoimmune disease. We report a 30‐year‐old woman who presented with fatigue, jaundice, pallor, and mucocutaneous bleeding.
Biruk T. Mengistie +6 more
wiley +1 more source
Variational Anatomy of the Segmental Branches of the Splenic Artery [PDF]
Journal of Clinical and Diagnostic Research, 2012 Background: The human spleen is highly vascular and friable and so it cannot be sutured. Total splenectomy is commonly done after a splenic injury, but it leads to a decrease in the immunity and thus it creates an altered haematological picture.
Prashant Nashiket Chaware +4 more
doaj
Коррекция гиперспленизма у пациентов с хирургическими осложнениями портальной гипертензии [PDF]
, 2015 ГИПЕРСПЛЕНИЗМ /хирТРОМБОЦИТОПЕНИЯ /хирСПЛЕНЭКТОМИЯэмболизация селезеночной артерииСЕЛЕЗЕНОЧНАЯ АРТЕРИЯЦИРРОЗ ПЕЧЕНИЦИРРОЗЫ ПЕЧЕНИКРОВОТЕЧЕНИЯГЕМОРРАГИИГИПЕРТЕНЗИЯ ...
Могилевец, Э. В.
core
Clinical &Translational Immunology, Volume 15, Issue 3, 2026.Familial haemophagocytic lymphohistiocytosis (FHL) is a rare, inherited granzyme–perforin system defect that predisposes individuals to haemophagocytic lymphohistiocytosis. This article presents two original case reports of FHL type 2, along with a comprehensive literature review. Together, these elements aim to enhance the current understanding of FHL
Nicolas Perrard +12 more
wiley +1 more source
Splenectomy in Patients with Chronic Idiopathic Thrombocytopenic Purpura
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2013 BACKGROUND AND OBJECTIVE: Splenectomy considered as second line therapy in management of patients with idiopathic thrombocytopenic purpura (ITP) whom did not respond to corticosteroid or the platelet decreased after corticosteroid cessation.
S Sedaghat +3 more
doaj
Comparative erythrocyte deformability investigations by filtrometry, slit-flow and rotational ektacytometry in a long-term follow-up animal study on splenectomy and different spleen preserving operative techniques: partial or subtotal spleen resection and spleen autotransplantation [PDF]
, 2018 K
Benkő, Ilona +13 more
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From Pharmaceutical to Biophysical Therapies: New Horizons in Inflammatory Bowel Disease Management
JCC Plus, Volume 1, Issue 2, March 2026.Important limitations exist in the current pharmacological landscape of Inflammatory Bowel Disease (IBD), such as variable response rates and treatment‐limiting adverse effects. In this review, we perform a critical assessment of the current literature on novel multimodal biophysical approaches showing alternative mechanisms of action to, and potential
Benedetta Ricchi +7 more
wiley +1 more source