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Anales de la Facultad de Medicina

versión impresa ISSN 1025-5583

Resumen

VALENZUELA-RODRIGUEZ, Germán; CABELLO LEON, Eduardo; YOZA YOSHIDAIRA, Max  y  PISCOYA RIVERA, Alejandro. Intestinal subocclusion and severe malnutrition in systemic sclerosis without scleroderma. An. Fac. med. [online]. 2023, vol.84, n.3, pp.322-324.  Epub 30-Sep-2023. ISSN 1025-5583.  http://dx.doi.org/10.15381/anales.v84i3.25662.

Systemic sclerosis sine Scleroderma is an uncommon form of systemic compromise of this disease, in the abscense of cutaneous manifestations. We present the case of a 71 years-old woman, body mass index (BMI) in 16.9 kg/m2, with history of hypothyroidism and chronic constipation, who goes to the emergency with pain, abdominal bloating, and nausea. An abdominopelvic tomography was made, reporting a collapse of the gastric chamber, some segments of intestinal loops distended with signs of fecalization in the small intestine. A colonoscopy described severe dolicocolon. We observed indurated plaques in left elbow and in both buttocks. Lab tests: ANA 1/640 with anticentromeric pattern, anticentromere antibodies = 227 U/mL (0-25), Anti-SCL-70 = 1.9 U/mL (0-25), anti-RNP = 0.1 U/mL (0-25). Peri-ungueal cappilaroscopy 200x showed mega capillaries. Clinical diagnosis was systemic sclerosis sine scleroderma. We initiated treatment with a high-fiber diet and parenteral nutrition for a week. The patient evolution was favorable.

Palabras clave : Scleroderma, Systemic; Malnutrition; Intestinal Obstruction.

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