2.Acrodermatitis Enteropathica-like Eruption Associated with Combined Nutritional Deficiency.
You Jeong KIM ; Mi Yeon KIM ; Hyung Ok KIM ; Myung Duck LEE ; Young Min PARK
Journal of Korean Medical Science 2005;20(5):908-911
We present here a case of acrodermatitis enteropathica-like eruption associated with essential free fatty acid and protein deficiencies as well as borderline zinc deficiency that occurred after Whipple's operation in a 31-yr-old woman. Her eruptions were improved not by zinc supplements alone, but her condition was improved by total parenteral nutrition including amino acids, albumin, lipid and zinc. Although we could not exactly decide which of the nutrients contributed the most to her manifestations, we inferred that all three elements in concert caused her dermatoses. This case shows that even though the patient's skin manifestations and laboratory results are suggestive of acrodermatitis enteropathica, the physicians should keep in mind the possibility that this disease can be associated with other nutritional deficiencies such as free fatty acid or protein deficiency.
Acrodermatitis/*diagnosis/*etiology
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Adult
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Fatty Acids, Essential/deficiency
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Female
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Humans
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Malnutrition/*diagnosis/*etiology
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Pancreatectomy/*adverse effects
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Protein-Losing Enteropathies/diagnosis/etiology
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Skin Diseases/*diagnosis/*etiology
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Zinc/deficiency
3.Factors related to outcomes in lupus-related protein-losing enteropathy.
Doo Ho LIM ; Yong Gil KIM ; Seung Hyeon BAE ; Soomin AHN ; Seokchan HONG ; Chang Keun LEE ; Bin YOO
The Korean Journal of Internal Medicine 2015;30(6):906-912
BACKGROUND/AIMS: Protein-losing enteropathy (PLE), characterized by severe hypoalbuminemia and peripheral edema, is a rare manifestation of systemic lupus erythematosus. This present study aimed to identify the distinctive features of lupus-related PLE and evaluate the factors related to the treatment response. METHODS: From March 1998 to March 2014, the clinical data of 14 patients with lupus PLE and seven patients with idiopathic PLE from a tertiary center were reviewed. PLE was defined as a demonstration of protein leakage from the gastrointestinal tract by either technetium 99m-labelled human albumin scanning or fecal alpha1-antitrypsin clearance. A positive steroid response was defined as a return of serum albumin to > or = 3.0 g/dL within 4 weeks after initial steroid monotherapy, and remission as maintenance of serum albumin > or = 3.0 g/dL for at least 3 months. A high serum total cholesterol level was defined as a level of > or = 240 mg/dL. RESULTS: The mean age of the lupus-related PLE patients was 37.0 years, and the mean follow-up duration was 55.8 months. Significantly higher erythrocyte sedimentation rate and serum total cholesterol levels were found for lupus PLE than for idiopathic PLE. Among the 14 patients with lupus PLE, eight experienced a positive steroid response, and the serum total cholesterol level was significantly higher in the positive steroid response group. A positive steroid response was associated with an initial high serum total cholesterol level and achievement of remission within 6 months. CONCLUSIONS: In lupus-related PLE, a high serum total cholesterol level could be a predictive factor for the initial steroid response, indicating a good response to steroid therapy alone.
Adult
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Aged
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Biomarkers/blood
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Cholesterol/blood
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Drug Therapy, Combination
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Edema/diagnosis/drug therapy/*etiology
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Female
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Glucocorticoids/therapeutic use
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Humans
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Hypoalbuminemia/diagnosis/drug therapy/*etiology
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Immunosuppressive Agents/therapeutic use
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Lupus Erythematosus, Systemic/*complications/diagnosis/drug therapy
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Male
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Middle Aged
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Protein-Losing Enteropathies/diagnosis/drug therapy/*etiology
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Remission Induction
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Risk Factors
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Serum Albumin/metabolism
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Tertiary Care Centers
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Time Factors
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Treatment Outcome
4.Chronic Non-granulomatous Ulcerative Jejunoileitis Assessed by Wireless Capsule Endoscopy.
Hyung Hun KIM ; You Sun KIM ; Kyung Sun OK ; Soo Hyung RYU ; Jung Hwan LEE ; Jeong Seop MOON ; Hyuck Sang LEE ; Hye Kyung LEE
The Korean Journal of Gastroenterology 2010;56(6):382-386
Chronic non-granulomatous jejunoileitis is a rare disease characterized by malabsorption, abdominal pain, and diarrhea that causes shallow ulcers in the small bowel. The etiology of chronic non-granulomatous jejunolieitis remains unknown. A 69-year-old man complained of abdominal pain and lower extremity edema. A 99m-Tc albumin scan showed increased radioactivity at the left upper quadrant, suggesting protein-losing enteropathy. A small bowel follow-through did not disclose any lesions. Wireless capsule endoscopy revealed several small bowel ulcers and strictures. A jejunoileal segmentectomy with end-to-end anastomosis was performed, and the histologic examination revealed non-granulomatous ulcers with focal villous atrophy. Ruling out all other possible diagnoses, we diagnosed our patient with chronic non-granulomatous ulcerative jejunoileitis. Postoperatively, the patient's abdominal pain and lower extremity edema improved, and the serum albumin normalized. This is the first case of chronic non-granulomatous ulcerative jejunoileitis localized by wireless capsule endoscopy and treated successfully with segment resection.
Abdominal Pain/etiology
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Aged
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Atrophy/diagnosis/etiology
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Capsule Endoscopy
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Chronic Disease
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Diagnosis, Differential
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Humans
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Ileitis/*diagnosis/pathology
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Intestine, Small/pathology
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Jejunal Diseases/*diagnosis/pathology
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Malabsorption Syndromes/diagnosis/pathology
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Male
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Mastectomy, Segmental
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Protein-Losing Enteropathies/diagnosis
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Technetium Tc 99m Aggregated Albumin/diagnostic use
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Ulcer/pathology