Results 1 to 10 of about 32,645 (198)

Hepatosplenomegaly and Pernicious Anaemia [PDF]

Journal of Clinical and Diagnostic Research, 2014
Sir, Pernicious anaemia (PA) is the end stage of atrophic gastritis which results in the loss of parietal cells in the fundus and body of the stomach. Loss of parietal cells is associated with the failure of intrinsic factor production and results in vitamin B12 deficiency and megaloblastic anaemia.
Turgay Ulas, Emel Yigit Karakas, Cemal Bes, Fatih Borlu, Hakan Buyukhatipoglu   +4 more
doaj   +3 more sources

Congenital Thrombocytosis, Hepatosplenomegaly, and Rash in a Term Neonate [PDF]

American Journal of Perinatology Reports
Objective Transient abnormal myelopoiesis (TAM) is a self-limited clonal myeloproliferative disorder seen almost exclusively in neonates with trisomy 21 and defined by circulating myeloblasts carrying N-terminal truncating GATA1 mutations.
Michal Mia Shalamov, Akshara Vadyala, Nirzar Parikh, Jessica Scerbo, Estephanie Rivero   +4 more
doaj   +2 more sources

Oral Lesion Management in Juvenile SLE with Hepatosplenomegaly

International Medical Case Reports Journal
Adrianus Surya Wira Rajasa,1 Wahyu Hidayat2 1Oral Medicine Residency Program, Faculty of Dentistry, Padjadjaran University, Bandung, Indonesia; 2Department of Oral Medicine, Faculty of Dentistry, Padjadjaran University, Bandung, IndonesiaCorrespondence ...
Wahyu Hidayat, Adrianus Rajasa
exaly   +2 more sources

The Spectrum of Clinical Manifestations of Serious Human Parvovirus B19 Infection in Children without any Underlying Diseases- A Case Series [PDF]

Journal of Clinical and Diagnostic Research, 2023
Human Parvovirus B19 causes mild to life-threatening illnesses, especially in immunosuppressed individuals. In the immunocompetent individuals, the severe spectrum of clinical manifestations of the virus infection is not widely known.
Subham Bhattacharya, Mrinal Kanti Das, Supratim Datta   +2 more
doaj   +1 more source

Hemophagocytic Lymphohistiocytosis Presenting as Neonatal Cholestasis: A Case Report [PDF]

Iranian Journal of Neonatology, 2023
Background:. Hemophagocytic lymphohistosis (HLH) is a life-threatening clinical syndrome that involves liver dysfunction and can range from mild dysfunction to severe fulminant insufficiency.
Raheleh Faramarzi, Azadeh Darabi, Seyed Morteza Rasti Sani, Hassan Boskabadi, Javad Mohamadi Taze Abadi   +4 more
doaj   +1 more source

Hypercalcaemia: An Extremely Rare Presentation of Hepatosplenic T-Cell Lymphoma

European Journal of Case Reports in Internal Medicine, 2021
Hypercalcaemia is a frequent finding in malignancies including lymphomas. However, there are no reports of hypercalcaemia in hepatosplenic T-cell lymphoma (HSTCL). HSTCL is a rare and aggressive neoplasm which is usually difficult to diagnose. We present
Sara Almeida Ramalho, Francisca Abecasis, Letícia Santos, Vanessa Leite, Diogo Gonçalves, Inês Pintassilgo, Ana Luisa Broa   +6 more
doaj   +1 more source

Brucellosis Infection- A Leukaemia Mimic [PDF]

Journal of Clinical and Diagnostic Research, 2023
Dear Editor, Brucellosis is multi-systemic infection with varied clinical presentation. Hematological manifestation of brucella includes, anaemia, thrombocytopenia, and pancytopenia with hepatosplenomegaly, lymphadenopathy which can be misdiagnosed as ...
Santosh Govind Rathod, Sauliha Yaseen
doaj   +1 more source

Combined Hereditary Spherocytosis and β-thalassemia trait: A Rare Co-existence [PDF]

Journal of Clinical and Diagnostic Research, 2018
Haemoglobinopathies are the commonest haemolytic disorders, prevalent in India and form a major bulk of patients in most of the haematology outpatient clinics.
Hanaganahalli Basavaiah Sridevi, Saraswathy Sreeram, Anupama Hegde, Prashantha Balanthimogru, Shrijeet Chakraborti   +4 more
doaj   +1 more source

Autosomal Recessive Polycystic Kidney Disease in a Child Complicated by Autoimmune Hemolytic Anemia: A Case Report [PDF]

Pediatric Sciences Journal (Egypt), 2023
Autosomal recessive polycystic kidney disease (ARPKD) is a rare genetic disorder that presents as an isolated polycystic renal disease in childhood, or associated with congenital hepatic fibrosis and/or Caroli disease.
Magd A. Kotb , Hend Abd El Baky , Shaimaa Sayed , Mohammed Al Komy, Marwa Onsy , Aya Aly , Andrew Tamer , Esraa Mohamed   +7 more
doaj   +1 more source

Niemann-Pick disease type B. Study of 3 cases and literature revision

Acta Pediátrica de México, 2014
Objective: To describe the course of type B Niemann-Pick disease (ENP-B) by following the evolution of three pediatric patients. Methods: Three patients, two of them male, age between two and eleven years, with type B Niemann-Pick disease were evaluated ...
Jorge Zarco-Román, Alva Nydia García-Pérez, Paulina Andrade-Aldama, Luis Carbajal-Rodríguez, Raymundo Rodríguez-Herrera   +4 more
doaj   +1 more source