Tuberous sclerosis complex presenting as primary intestinal lymphangiectasia: A case report
نویسندگان
چکیده
منابع مشابه
Tuberous sclerosis complex: A case report
Tuberous Sclerosis Complex (TSC) was first described in the late 1800s as a relative of neurofibromatosis, but it has since been identified as a discrete disorder. Patients with TSC typically present with facial adenomas, seizure disorder, and a developmental disability. The syndrome is caused by mutations in either chromosomes 9 or 16, both of which code for cell development and maturation. Th...
متن کاملIntestinal Lymphangiectasia a Case Report
A 28 year old woman with protein losing enteropathy due to intestinal lymphangiectasia is presented. The patient had diarrhoea, oedema restricted to the lower extremities, hypoproteinemia and an abnormal radiological appearance of the small intestines. Jejunal biopsy and the histopatho-logy report of the resected jejunum showed dilated lymphatics in the submucosa. Post-operatively patient showe...
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Background Tuberous Sclerosis Complex (TSC), and Spinal Muscular Atrophy (SMA) are two inherited disorders while they are genetically independent. TSC is characterized by the formation of multiple hamartomas in nearly all organs. SMA is a destructive neurological disorder leading to progressive muscular weakness and atrophy. Case Presentation</e...
متن کاملTuberous sclerosis complex presenting as pulmonary lymphangioleiomyomatosis - a clinicoradiological diagnosis
Tuberous sclerosis complex (TSC) manifests predominantly as a neurocutaneous disorder. Lymphangioleiomyomatosis (LAM) is a rare pulmonary manifestation of TSC. Imaging evaluation plays an important role in the assessment of patients with tuberous sclerosis complex. In newly diagnosed patients, it helps not only to confirm the diagnosis of TSC, but also helps in identifying clinically significan...
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Sir: Tuberous sclerosis complex (TSC) is a rare autosomal dominant disease characterized by hamartomatous lesions in several organs. TSC-related pulmonary manifestations comprise several pathological conditions, such as lymphangioleiomyomatosis (LAM), multifocal micronodular pneumocyte hyperplasia (MMPH), clear cell sugar tumour, angiomyolipoma and micronodular ⁄ interstitial clear cell LAM-lik...
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ژورنال
عنوان ژورنال: World Journal of Clinical Cases
سال: 2020
ISSN: 2307-8960
DOI: 10.12998/wjcc.v8.i10.1995