Results 11 to 20 of about 3,502,714 (163)
Protein-Losing Enteropathy in Primary Lymphangiectasia
Teaching Point: Intestinal lymphangectasia should be evoked in the rare context of protein-losing enteropathy with low-attenuation thickening of the bowel wall.
Bernard Crutzen, Pierre-Antoine Poncelet
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Neuroblastoma presenting as protein-losing enteropathy
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.
T Coşkun +3 more
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Protein-Losing Enteropathy in Ulcerative Colitis
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
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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.
Katsuya Endo +15 more
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Protein-Losing Enteropathy in the Setting of Severe Iron Deficiency Anemia
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
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Allergic enterocolitis and protein-losing enteropathy as the presentations of manganese leak from an ingested disk battery: A case report [PDF]
Introduction Disk battery ingestions can lead to serious complications including airway or digestive tract perforation, blood vessel erosions, mediastinitis, and stricture formation.
Altaf Muhammad A +2 more
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Protein-losing enteropathy demonstrated on Tc-99m HSA [PDF]
No abstrac available.
P Mpikashe, M M Sathekge, B J Meyer
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A rare cause of protein-losing enteropathy and growth retardation in infancy: infantile systemic hyalinosis [PDF]
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.
Benal Büyükgebiz +3 more
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Disseminated Langerhans' cell histiocytosis and massive protein-losing enteropathy
Symptomatic involvement of the gastrointestinal (GI) tract as a prominent symptom in Langerhans' cell histiocytosis (LCH) is uncommon, occurring in less than 1 to 5% of all cases, even when the disease is in its disseminated form.
Santos-Machado T.M. +7 more
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Protein-losing enteropathy is one of the most feared complications of the Fontan circulation. The diagnosis of protein-losing enteropathy in this setting should prompt a thorough investigation for the presence of a treatable hemodynamic impairment.
Milan Djukic +5 more
doaj +1 more source

