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A new species of (Crustacea, Mysida) from the Canary and Cape Verde archipelagos.
Biodivers Data J
December 2024
Zentrum für Public Health, Medizinische Universität Wien, Vienna, Austria Zentrum für Public Health, Medizinische Universität Wien Vienna Austria.
Background: Within the subfamily Leptomysinae (fam. Mysidae), the tribe Mysidopsini has five here acknowledged genera and 74 extant species. It embraces the genera with six species from the coasts of the NW-Atlantic (Narragansett Bay to Florida), the Caribbean and Gulf of Mexico; with two species from the SW-Atlantic off Brazilian shores and from the Pacific coast of Ecuador; with three species from the Caribbean, Gulf of California and southern California; with ten species from the Atlantic coasts of the USA to Brazil, Caribbean, Gulf of Mexico and E-Pacific from California to Panama; and, finally, the globally occurring .
View Article and Find Full Text PDFGastrointestinal Alpha Heavy Chain Disease With Persistent Colonization and Refractory Giardiasis.
ACG Case Rep J
August 2024
Department of Gastroenterology and Hepatobiliary Diseases, New York Medical College, Valhalla, NY.
Alpha heavy chain disease (αHCD) is a rare variant of the mucosa-associated lymphoid tissue lymphoma characterized by expression of a monotypic truncated immunoglobulin α heavy chain. αHCD frequently involves the gastrointestinal (GI) tract, and its pathogenesis has been linked to clonal B-cell expansion from chronic immune stimulation by infectious agents. We report a rare case of GI αHCD with 5 concomitant pathogens identified on a GI multiplex real-time polymerase chain reaction panel, featured by persistent colonization and refractory giardiasis.
View Article and Find Full Text PDFUpdates on the Diagnosis and Management of Fibrillary Glomerulonephritis.
Adv Kidney Dis Health
July 2024
Division of Nephrology, Lenox Hill Hospital, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, New York, NY. Electronic address:
Article Synopsis
- Fibrillary glomerulonephritis (FGN) is a rare kidney condition common in middle-aged adults, usually leading to severe kidney failure, proteinuria, and high blood pressure, and can be linked to autoimmune diseases and infections like hepatitis C.
- The diagnosis of FGN is confirmed by renal biopsy showing unique fibrils and is aided by DnaJ homolog subfamily B member 9 immunostaining, while the disease has various atypical forms.
- Treatment options, particularly immunosuppression with drugs like rituximab, vary in effectiveness, and FGN often progresses to end-stage kidney disease within 2-4 years, where kidney transplantation is a potential solution, though recurrence in transplanted kidneys
Treatment-Resistant Immunoproliferative Small Intestinal Disease (IPSID) Leading to Lymphoma.
Cureus
June 2024
Department of Gastroenterology and Hepatology, Rutgers New Jersey Medical School, Newark, USA.
Article Synopsis
- Immunoproliferative small intestinal disease (IPSID) is a type of MALT lymphoma, mainly affecting the proximal small intestine and linked to chronic infection, causing symptoms like malabsorption and weight loss.
- A case study of a 50-year-old Nigerian woman highlights the diagnostic challenges of IPSID, as her symptoms were initially misattributed to other conditions despite multiple antibiotic treatments.
- The patient's condition progressed from initial symptom relief with antibiotics to requiring chemotherapy after developing lymphoma, illustrating the complexities of managing IPSID effectively.
Renal epithelioid angiomyolipoma: A case report.
Oncol Lett
September 2023
Department of Urology, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Jinan, Shandong 250014, P.R. China.
Epithelioid angiomyolipoma (EAML) of the kidney is an uncommon neoplasm with malignant potential. It can occur sporadically or be associated with tuberous sclerosis. EAML is a monotypic variant of angiomyolipoma (AML), which is classified as neoplasm of the perivascular epithelioid cell or perivascular epithelioid cell tumor.
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