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1.
Saudi Medical Journal. 2014; 35 (9): 1120-1122
in English | IMEMR | ID: emr-154781

ABSTRACT

We present a case of a 3 /2 -year-old girl diagnosed as Proteus syndrome with severe cosmetic disfigurement-macrodactyly, hemi-hypertrophy of the face and limbs, megalencephaly, lymph edema of both hands and feet along with severe global developmental delay. She was found to have severe recalcitrant epilepsy and also primary hypothyroidism; the association of which is not mentioned in the previous literature

2.
Saudi Medical Journal. 2003; 24 (10): 1130-1132
in English | IMEMR | ID: emr-64459

ABSTRACT

Abdominal cystic lymphangioma is a very rare congenital tumor of lymphatic origin. It usually appears in the pediatric age and frequently presents with non-specific symptoms and deceptive signs causing, at times, diagnostic dilemmas. Ultrasonography and computer tomography imaging are considered the diagnostic modalities of choice. Two cases of mesenteric cystic lymphangioma, one presenting as perforated appendicitis and the other as recurrent gastritis, are reported. Infection in the first and volvulus in the second case is behind the mode of presentation. The diagnostic approach and treatment are described with emphasis on the operative tactic applied for upper jejunal resection. A high index of suspicion, accuracy and repeated physical examination and, most important, the liberal use of ultrasonography in all cases of unclear abdominal illness may contribute considerably to a correct diagnosis and decreased morbidity


Subject(s)
Humans , Male , Female , Lymphangioma, Cystic/surgery , Mesentery , Peritoneal Neoplasms/diagnosis , Peritoneal Neoplasms/surgery , Gastritis/diagnosis , Recurrence , Lymphatic System/pathology
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