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199 Possible Causes for Liver Hemangioma, Polycystic Kidney Disease

  • Hereditary Hemorrhagic Telangiectasia

    Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people. Clinical diagnosis of HHT is made when a person presents three of the following four criteria: family history, recurrent nosebleeds, mucocutaneous telangiectasis, and[…][ncbi.nlm.nih.gov]

  • Von Hippel-Lindau Disease

    On abdominal ultrasonography, liver hemangiomas and pancreatic cysts were seen, confirmed by abdominal computerized tomography (CT).[ncbi.nlm.nih.gov] Differential diagnosis Differential diagnoses include multiple endocrine neoplasia, neurofibromatosis, polycystic kidney disease, tuberous sclerosis, Birt-Hogg-Dube syndrome[orpha.net] (MEN type 2) Multiple paraganglioma syndrome Neurofibromatosis Pheochromocytoma Autosomal dominant polycystic kidney disease (ADPKD) Birt-Hogg-Dube (BHD) syndrome Tuberous[emedicine.medscape.com]

  • Cholangiocarcinoma

    Atypical hepatic hemangioma. US, CT, MRI and Tc-99m RBC liver scans were performed.[ncbi.nlm.nih.gov] (a rare congenital disorder of the intrahepatic bile ducts associated with autosomal recessive polycystic kidney disease where the bile ducts become chronically dilated).[patient.info] Histopathologic examination of the liver lesions revealed nodular cirrhosis and atypical hyperplasia of liver cells with cavernous hemangioma, where numerous old Schistosoma[ncbi.nlm.nih.gov]

  • Chylous Ascites

    Hilzenrat Chylous ascitis secondary to giant liver hemangioma [2] T. Almakdisi,S. Massoud,G. Makdisi Lymphomas and chylous ascitis: Review of the literature [3] M.[revistagastroenterologiamexico.org] Autosomal recessive polycystic kidney disease; radiologic-pathologic correlation . RadioGraphics 2000; 20 : 837–855.[nature.com] He was a known case of polycystic kidney disease, diagnosed 15 years earlier.[sjkdt.org]

  • Hepatic Rupture

    […] rupture including primary liver cancer, cirrhosis, liver adenoma, secondary liver cancer and liver hemangioma as causes of rupture).[wjgnet.com] kidney disease.[surgicalcasereports.springeropen.com] Results and discussion: Although hemangiomas are rare, spontaneous rupture of these liver lesions has been well-described.[mdmag.com]

  • Megacystis - Megaureter Syndrome

    Bazzocchi 8 Liver Hemangioma V. Vilgrain and G. Brancatelli 9 Focal Nodular Hyperplasia A. Filippone, R. Basilico, F. Di Fabio, and L.[books.google.com] Renal Cyst Parapelvic/Peripelvic Cyst Autosomal Dominant Polycystic Kidney Disease Polycystic Kidney Disease, Autosomal Recessive Multicystic Dysplastic Kidney Acquired Cystic[elsevier.com] kidney disease 2725 Autosomal dominant (AD) polycystic kidney disease type I 2739 Autosomal dominant (AD) polycystic kidney disease type II 2741 Autosomal recessive (AR)[srr.scot.nhs.uk]

  • Penoscrotal Transposition

    &60;p&62;Hemangiomas are usually superficial, localized, and commonly involve the head&60;br /&62;or neck, although up to 30% may be seen in the liver.[ingentaconnect.com] Type III is due to Autosomal dominant polycystic kidney disease (ADPKD) linked to mutations in the genes PKD1 and PKD2.[omicsonline.org] Hemangioma involving the&60;br /&62;glans penis is extremely rare. A patient with red swelling on the glans penis was&60;br /&62;admitted for circumcision to our clinic.[ingentaconnect.com]

  • Allan-Herndon-Dudley Syndrome

    […] determine likelihood of CH: 1. 20% of CH was postdates 42 weeks 2. maternal autoimmune thyroid disease, iodine deficient diet. 3. fetal exposure to antithyroid drugs 4. liver[quizlet.com] kidney disease Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia popliteal pterygium syndrome postsurgical hypothyroidism[rgd.mcw.edu] Liver hemangiomas - There are reports of congenital liver hemangiomas that produce large amounts of the enzyme type 3 iodothyronine deiodinase.[ojrd.biomedcentral.com]

  • Klippel-Trenaunay-Weber Syndrome

    A case of Klippel-Trenaunay-Weber Syndrome (KTWS) in a 2.5-year-old girl with congenital hemihypertrophy, nevus flammeus and liver hemangioma is presented.[ncbi.nlm.nih.gov] A case of polycystic kidney disease (PKD) associated with Klippel-Trenaunay-Weber syndrome is described.[ncbi.nlm.nih.gov] The hemangioma may be confined to the skin or advanced to the bone and muscle, and organs such as the liver, spleen, bladder, large bowel, and others.[symptoma.com]

  • Hemoperitoneum

    Initially, the computed tomography finding was interpreted as liver hemangioma.[ncbi.nlm.nih.gov] kidney disease (ADPKD).[academic.oup.com] Among the causes of primary kidney disease, the most common ones were diabetic nephropathy (22.7%), polycystic renal disease (6.1%), and systemic amiloidosis (8.3%).[revistanefrologia.com]

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