{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,1,26]],"date-time":"2024-01-26T01:02:14Z","timestamp":1706230934190},"reference-count":10,"publisher":"Walter de Gruyter GmbH","issue":"2","license":[{"start":{"date-parts":[[2017,6,1]],"date-time":"2017-06-01T00:00:00Z","timestamp":1496275200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2017,6,30]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Peliosis hepatis (PH) is a rare, benign condition of the liver characterized by the presence of blood-filled lacunar spaces in the parenchyma. It usually has a chronic presentation and is a rare cause of portal hypertension reported in adult patients. Its etiology is diverse and ranges from infectious agents to tumors to toxic substances and anabolic steroids; however, the cause remains unclear in 25\u201350% of patients. Similarly, the symptomatology and imaging findings are diverse. Biopsy is the definitive test to diagnose the condition. Herein, we present a case of a young female presenting in her seventh month of gestational amenorrhea with signs of portal hypertension and subsequently diagnosed to have PH. She was managed conservatively and delivered her baby normally. Later, she presented with spontaneous bacterial peritonitis and hepatic encephalopathy and developed hepatorenal syndrome. She later succumbed to her illness. The condition should be kept in the differential diagnosis of the atypical liver masses and liver diseases causing portal hypertension.<\/jats:p>","DOI":"10.1515\/jtim-2017-0023","type":"journal-article","created":{"date-parts":[[2017,7,3]],"date-time":"2017-07-03T08:08:10Z","timestamp":1499069290000},"page":"132-134","source":"Crossref","is-referenced-by-count":3,"title":["Peliosis hepatis complicating pregnancy: A rare entity"],"prefix":"10.1515","volume":"5","author":[{"given":"Muhammad Osama","family":"Butt","sequence":"first","affiliation":[{"name":"Departments of Hepatogastroenterology , Sindh Institute of Urology and Transplantation (SIUT) , Karachi - 74200 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nasir Hassan","family":"Luck","sequence":"additional","affiliation":[{"name":"Departments of Hepatogastroenterology , Sindh Institute of Urology and Transplantation (SIUT) , Karachi - 74200 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Syed Mujahid","family":"Hassan","sequence":"additional","affiliation":[{"name":"Departments of Hepatogastroenterology , Sindh Institute of Urology and Transplantation (SIUT) , Karachi - 74200 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zaigham","family":"Abbas","sequence":"additional","affiliation":[{"name":"Departments of Hepatogastroenterology , Sindh Institute of Urology and Transplantation (SIUT) , Karachi - 74200 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Muhammed","family":"Mubarak","sequence":"additional","affiliation":[{"name":"Departments of Histopathology , Sindh Institute of Urology and Transplantation (SIUT) , Karachi - 74200 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","published-online":{"date-parts":[[2017,6,30]]},"reference":[{"key":"2023042508112910494_j_jtim-2017-0023_ref_001_w2aab3b8c33b1b7b1ab2b1b1Aa","doi-asserted-by":"crossref","unstructured":"Vignaux O, Legmann P, de Pinieux G, Chaussade S, Spaulding C, Couturier D, et al. Hemorrhagic necrosis due to peliosis hepatis: Imaging findings and pathological correlation. Eur Radiol 1999;9:454-6.","DOI":"10.1007\/s003300050691"},{"key":"2023042508112910494_j_jtim-2017-0023_ref_002_w2aab3b8c33b1b7b1ab2b1b2Aa","unstructured":"Spech HJ, Liehr H. Peliosis hepatis. A clinical status inventory. Z Gastroenterol 1982;20:710-21."},{"key":"2023042508112910494_j_jtim-2017-0023_ref_003_w2aab3b8c33b1b7b1ab2b1b3Aa","unstructured":"Nieves Cereceda C, Solis Herruzo JA, Munoz-Yague MT, De Blas C. Hepatic peliosis. Review of the literature. Rev Esp Enferm Apar Dig 1989;75:205-11."},{"key":"2023042508112910494_j_jtim-2017-0023_ref_004_w2aab3b8c33b1b7b1ab2b1b4Aa","doi-asserted-by":"crossref","unstructured":"DeLeve LD. Vascular liver diseases. Curr Gastroenterol Rep 2003;5:63-70.","DOI":"10.1007\/s11894-003-0011-0"},{"key":"2023042508112910494_j_jtim-2017-0023_ref_005_w2aab3b8c33b1b7b1ab2b1b5Aa","doi-asserted-by":"crossref","unstructured":"Cavalcanti R, Pol S, Carnot F, Campos H, Degott C, Driss F, et al. Impact and evolution of peliosis hepatis in renal transplant recipients. Transplantation 1994;58:315-6.","DOI":"10.1097\/00007890-199408000-00011"},{"key":"2023042508112910494_j_jtim-2017-0023_ref_006_w2aab3b8c33b1b7b1ab2b1b6Aa","doi-asserted-by":"crossref","unstructured":"Hyodo M, Mogensen AM, Larsen PN, Wettergren A, Rasmussen A, Kirkegaard P, et al. Idiopathic extensive peliosis hepatis treated with liver transplantation. J Hepatobiliary Pancreat Surg 2004;11:371-4.","DOI":"10.1007\/s00534-004-0908-5"},{"key":"2023042508112910494_j_jtim-2017-0023_ref_007_w2aab3b8c33b1b7b1ab2b1b7Aa","doi-asserted-by":"crossref","unstructured":"Kim EA, Yoon KH, Jeon SJ, Cai QY, Lee YW, Yoon SE, et al. 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Macroscopic and microscopic findings of livers in malignant hematologic disorders, biopsied under peritoneoscopy. 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