Results 11 to 20 of about 2,210 (159)

Protein‐losing enteropathy as the first presentation of systemic lupus erythematosus: A case report from Sudan

open access: yesClinical Case Reports, 2023
Key Clinical Message In low‐ and middle‐income countries, protein‐losing enteropathy is a diagnosis of exclusion. SLE should be on the list of differential diagnoses of protein‐losing enteropathy, especially if the patient had a long history of GI ...
Noon Mohymeed   +6 more
core   +2 more sources

Lupus-related protein-losing enteropathy associated with pseudo-pseudo Meigs’ syndrome and successfully treated with hydroxychloroquine

open access: yesRomanian Journal of Internal Medicine, 2022
We herein report the first case of lupus-related protein-losing enteropathy associated with pseudo-pseudo Meigs’ syndrome. Lupus-related protein-losing enteropathy and pseudo-pseudo Meigs’ syndrome are extremely rare complications in patients with ...
Ishihara Masayuki   +8 more
core   +2 more sources

Protein-Losing Enteropathy in Primary Lymphangiectasia.

open access: yesJournal of the Belgian Society of Radiology, 2020
TEACHING POINT Intestinal lymphangectasia should be evoked in the rare context of protein-losing enteropathy with low-attenuation thickening of the bowel ...
Poncelet, Pierre-Antoine   +1 more
core   +2 more sources

NEUROBLASTOMA PRESENTING AS PROTEIN-LOSING ENTEROPATHY

open access: yesThe Turkish Journal of Pediatrics, 1992
Protein - losing enteropathy is often reported to be associated with malignancies such as Hodgkin's disease, non - Hodgkin's lymphoma, and mesenteric mesenchymoma, but it seldom complicates neuroblastoma.
BUYUKPAMUKCU, M   +3 more
core   +2 more sources

Suggestive Diagnostic Process in a Case of Multiple Myeloma with Gastrointestinal Immunoglobulin Light-Chain Amyloidosis Accompanied by Protein-Losing Enteropathy

open access: yesCase Reports in Gastrointestinal Medicine, 2021
Multiple myeloma is a type of plasma cell neoplasm that produces monoclonal immunoglobulin. Multiple myeloma is known to cause immunoglobulin light-chain (AL) amyloidosis, which frequently involves the kidney and heart.
Takayuki Kogure   +15 more
core   +2 more sources

Protein-Losing Enteropathy in Ulcerative Colitis

open access: yesCase Reports in Gastroenterology, 2012
Protein-losing enteropathy (PLE) is a debilitating potential complication of ulcerative colitis (UC). We report a case of PLE in a 26-year-old male patient with UC.
Ryan Ungaro   +3 more
core   +2 more sources

Protein-Losing Enteropathy in the Setting of Severe Iron Deficiency Anemia

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2018
A 20-month-old boy presented with a 2-week history of pallor and progressive abdominal distention. Nutritional history revealed long-standing excessive cow milk intake.
Jessica Lacy Yasuda MD   +1 more
core   +2 more sources

Association of Protein-losing Enteropathy and Cryoglobulinaemia

open access: yesScandinavian Journal of Gastroenterology, 2003
We describe a case of protein-losing enteropathy in association with cryoglobulinaemia. No underlying disorder could be definitively diagnosed, but several clinical and laboratory findings suggested an immune mediated or autoimmune disorder. We propose that the mechanism of the protein-losing enteropathy in our case was immune complex formation ...
Samarkos, M   +5 more
openaire   +4 more sources

Allergic enterocolitis and protein-losing enteropathy as the presentations of manganese leak from an ingested disk battery: A case report

open access: yesJournal of Medical Case Reports, 2008
Introduction Disk battery ingestions can lead to serious complications including airway or digestive tract perforation, blood vessel erosions, mediastinitis, and stricture formation.
Praveen S Goday   +5 more
core   +2 more sources

A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis

open access: yesThe Turkish Journal of Pediatrics, 2003
Infantile systemic hyalinosis is a rare, progressive, fatal condition with a presumably autosomal recessive mode of inheritance. It is characterized. by widespread deposition of hyaline material in many tissues.
Buyukgebiz, B   +3 more
core   +3 more sources

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