Results 1 to 10 of about 81,190 (299)

Sarcoidosis presenting as isolated massive splenomegaly: A case report

Clinical Case Reports
Key Clinical Message Sarcoidosis is a systemic granulomatous disease with an unknown cause, marked by the presence of noncaseating granulomas in the affected organs.
Melissa Kyriakos Saad, Imad El Hajj, Elias Saikaly   +2 more
doaj   +1 more source

Investigation and Analysis of Iron-Deficiency Anemia Complicated by Splenomegaly

International Journal of General Medicine, 2021
Yan-hui Wei,1 Yu-zhuo He,2 Xiao-yan Guo,1 Xiao-yan Lin,2 Hong-bin Zhu,2 Xue-jun Guo2 1Department of Graduate School, Xinxiang Medical University, Xinxiang, Henan Province, 453003, People’s Republic of China; 2Department of Hematology, Puyang Oilfield ...
Wei Y, He Y, Guo X, Lin X, Zhu H, Guo X
doaj  

A misleading miscellanea: a COVID-19 patient with fever and cytopenia

Italian Journal of Medicine
Complex clinical cases characterized by the coexistence of multiple pathologies and, consequently, multiple signs and symptoms shared by various pathological entities can hide pitfalls that may lead to incorrect diagnostic conclusions due to cognitive ...
Pietro Bocchi, Lara Zerbini, Elisa Gnappi, Maurizio Ziliotti, Marco Pesci, Luisa Craviotto, Michele Meschi   +6 more
doaj   +1 more source

Surgical treatment of spontaneous spleen rupture in patients with splenomegalia [PDF]

Scripta Medica, 2018
Spontaneous spleen rupture rarely occurs, and is primarily present in patients with splenomegaly. This is a life-threatening condition that, without adequate surgical treatment, always ends lethally.
Đeri Jugoslav, Simatović Milan, Vujanović Vojo, Topić Duško   +3 more
doaj  

Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) in Common Variable Immunodeficiency (CVID): A Multicenter Retrospective Study of Patients From Italian PID Referral Centers

Frontiers in Immunology, 2021
Background: Granulomatous and Lymphocytic Interstitial Lung Diseases (GLILD) is a severe non-infectious complication of Common Variable Immunodeficiency (CVID), often associated with extrapulmonary involvement.
Francesco Cinetto, Francesco Cinetto, Riccardo Scarpa, Riccardo Scarpa, Maria Carrabba, Davide Firinu, Vassilios Lougaris, Vassilios Lougaris, Helena Buso, Helena Buso, Giulia Garzi, Sabrina Gianese, Sabrina Gianese, Valentina Soccodato, Alessandra Punziano, Gianluca Lagnese, Giulio Tessarin, Giulio Tessarin, Giulia Costanzo, Nicholas Landini, Stefania Vio, Maria Pia Bondioni, Dario Consonni, Carolina Marasco, Stefano Del Giacco, Marcello Rattazzi, Marcello Rattazzi, Angelo Vacca, Alessandro Plebani, Alessandro Plebani, Giovanna Fabio, Giuseppe Spadaro, Carlo Agostini, Carlo Agostini, Isabella Quinti, Cinzia Milito   +35 more
doaj   +1 more source

Concomitant splenic artery ligation has no preventive effect on left‐sided portal hypertension following pancreaticoduodenectomy with the resection of the portal and superior mesenteric vein confluence for pancreatic ductal adenocarcinoma

Annals of Gastroenterological Surgery, 2022
Background Left‐sided portal hypertension (LSPH) caused by splenic vein (SV) division in pancreaticoduodenectomy (PD) with portal vein (PV) resection remains challenging. The current study aimed to investigate the efficacy of splenic artery (SA) ligation
Kazuyuki Gyoten, Shugo Mizuno, Motonori Nagata, Takahiro Ito, Aoi Hayasaki, Yasuhiro Murata, Akihiro Tanemura, Naohisa Kuriyama, Masashi Kishiwada, Hiroyuki Sakurai   +9 more
doaj   +1 more source

Early Onset Felty Syndrome in Rheumatoid Arthritis: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Felty syndrome is a rare and serious complication of Rheumatoid Arthritis (RA), characterised by a triad of RA, splenomegaly (enlarged spleen), and neutropenia (low neutrophil count).
Abhishek Kumar, P Harikrishnan, Manish Manrai, Abhinav Kumar   +3 more
doaj   +1 more source

Primary splenic diffuse large B-cell lymphoma: a case report

European Journal of Case Reports in Internal Medicine, 2023
Primary splenic lymphoma (PSL) is a rare disease and an improbable cause of splenomegaly or splenic nodules. On the contrary, splenic secondary involvement as part of an advanced lymphoproliferative disorder is more common.
Nuno Maia Neves, Ana Pestana Lopes, Susana Carvalho Coelho, Anabela Raimundo, Maria Manuela Mafra, Alexandra Bayão Horta   +5 more
doaj   +1 more source

Lymphadenopathy and Splenomegaly

, 2005
Lymphadenopathy and splenomegaly are benign and malignant processes that can produce common findings in children and it is important to distinguish between the two so that appropriate management can be undertaken. Lymphadenopathy might be caused by proliferation of cells intrinsic to the node, such as lymphocytes, plasma cells, monocytes or histiocytes
openaire   +1 more source

Prevalence of Gaucher’s Disease in a Hematology Outpatient Clinic

Journal of Contemporary Medicine, 2020
Objective: Gaucher’s disease (GD) is a disease caused by glucocerebrosidase enzyme deficiency and characterized by glucoceramide accumulation in the reticuloendothelial system.
Didar Yanardağ Açık, Bilal Aygun
doaj   +1 more source