Results 11 to 20 of about 44,988 (225)
Structural and functional hepatic factors as prognostic indicators in children with Langerhans cell histiocytosis [PDF]
Frontiers in OncologyBackground and aimLangerhans cell histiocytosis (LCH) is a clonal myeloid neoplasm with variable outcomes; hepatic involvement is uniformly classified as high-risk.
Seham Hassan +6 more
doaj +2 more sources
Case Report: Systemic amyloidosis unmasked by progressive hepatomegaly after splenectomy for non-traumatic spleen rupture in a patient with chronic liver disease [PDF]
Frontiers in MedicineBackgroundNon-traumatic splenic rupture (NSR) is a rare manifestation of systemic amyloid light-chain amyloidosis (AL amyloidosis), a plasma cell dyscrasia best known for its cardiorenal involvement.
Li-Ping Sheng +10 more
doaj +2 more sources
Pediatric Care Online, 2020 Key Points Hepatomegaly results from increase in the number or size of cells in the liver. Liver span correlates more strongly with hepatomegaly than projection below the costal margin. As a sign, not itself a disease, hepatomegaly can result from broad categories of disorders with an extensive differential diagnosis.
K. Gupta, P. Carmichael, A. Zumla
+5 more sources
Chronic neutrophilic leukemia: A case report [PDF]
Romanian Medical Journal, 2023 Objectives. We present a case report of a patient with malaise, abdominal pain, and vomiting, later underwent bone marrow biopsy and found to have CNL with no genetic mutation. Case presentation.
Rahmat Cahyanur +6 more
doaj +1 more source
Clinical fnd epidemiological features of measles by adults in modern period
Журнал инфектологии, 2021 Positive results have been achieved during the implementation of the measles elimination program in the Russian Federation and in the Northwestern Federal District (NWFD).
V. V. Basina +4 more
doaj +1 more source
Primary Amyloidosis - In a Case with Normal Plasma Cell Counts [PDF]
Journal of Clinical and Diagnostic Research, 2017 Amyloidosis is a group of disease that is characterized by the deposition of extracellular abnormal proteinaceous material (amyloid), in various organs. Amyloidosis involving the liver is common, and the radiological findings are often nonspecific.
POOJA TREHAN +4 more
doaj +1 more source
Postgraduate Medical Journal, 2007 A female publican in her 60s presented to clinic with abnormal liver function tests: bilirubin 17 μmol/l (normal range (NR) 0–17 μmol/l), alanine transaminase (ALT) 73 IU/l (NR 0–70 IU/l), alkaline phosphatase (ALP) 463 IU/l (NR 42–128 IU/l), γ glutamyl transferase (GGT) 784 IU/l (NR 2–35 IU/l), albumin 35 g/l (NR 35–50 g/l), prothrombin time (PT) 11.0
D, Joshi +4 more
openaire +2 more sources
Massive Hepatomegaly Secondary to Amyloidosis with Normal Liver Chemistries
Case Reports in Gastroenterology, 2020 Amyloid light chain (AL) amyloidosis is a disease of misfolded, fibrous proteins, either kappa or lambda subtype, that can be deposited into one or more organs, caused by a proliferation of plasma cells.
Sarah Doe-Williams +2 more
doaj +1 more source
The NADPH oxidase NOX4 regulates redox and metabolic homeostasis preventing HCC progression
Hepatology, EarlyView., 2022 Loss of NOX4 in HCC tumor cells induces metabolic reprogramming in a Nrf2/MYC‐dependent manner to promote HCC progression. Abstract Background and Aims The NADPH oxidase NOX4 plays a tumor‐suppressor function in HCC. Silencing NOX4 confers higher proliferative and migratory capacity to HCC cells and increases their in vivo tumorigenic potential in ...
Irene Peñuelas‐Haro +14 more
wiley +1 more source
Memorias do Instituto Oswaldo Cruz, 2009 Most cases of acute acquired toxoplasmosis (AAT) are oligosymptomatic and self-limited. Therefore, these infections rarely indicate treatment. Prospective studies of AAT patients are rare in the medical literature.
ES Neves +8 more
doaj +1 more source