Publications by authors named "Nerea Torrecilla Idoipe"
Article Synopsis
- - Mucopolysaccharidosis type IIIB is a lysosomal storage disease that results from a deficiency of the enzyme N-acetyl-alpha-d-glucosaminidase, leading to the buildup of heparan sulfate in tissues.
- - An 8-year-old patient with this condition experienced chronic diarrhea linked to intestinal lymphangiectasia, which improved after starting a low-fat diet with medium-chain triglycerides.
- - The cause of chronic diarrhea in Mucopolysaccharidosis type IIIB is still unclear, but the presence of intestinal lymphangiectasia in these patients should be looked into, and dietary modifications may enhance their quality of life.
A healthy 10-year-old boy presented with plaque-like cutaneous mucinosis (PCM) on his back. Cutaneous biopsy was followed by progressive resolution of the skin lesion. Pediatric PCM could differ clinically from the adult form.
View Article and Find Full Text PDFAdenosquamous carcinoma is a rare colorectal tumor with few cases described in the literature; no children have been reported. A 12-year-old-girl presented tenesmus, diarrhea, and iron deficiency anemia. Intestinal bowel disease was suspected, colonoscopy and biopsy were performed and the diagnosis was a squamous cell carcinoma.
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