Pneumatocele Development after Deceased-Donor Liver Transplantation for Multiple Hepatic Cysts due to Autosomal Dominant Polycystic Kidney Disease: A Case Report

被引:0
|
作者
Yoshiyama, Atsushi [1 ]
Kawashima, Mitsuaki [1 ]
Nagata, Sodai [1 ]
Fukushima, Takahito [1 ]
Aze, Koji [1 ]
Cong, Yue [1 ]
Nakao, Keita [1 ]
Nakao, Masayuki [1 ]
Toyokawa, Gouji [1 ]
Konoeda, Chihiro [1 ]
Hasegawa, Kiyoshi [2 ]
Sato, Masaaki [1 ]
机构
[1] Univ Tokyo Hosp, Dept Thorac Surg, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
[2] Univ Tokyo Hosp, Dept Surg, Hepatobiliary Pancreat Surg Div, Tokyo, Japan
来源
SURGICAL CASE REPORTS | 2025年 / 11卷 / 01期
关键词
pneumatocele; pulmonary cyst; liver transplantation; atelectasis; positive-pressure ventilation; LOBECTOMY;
D O I
10.70352/scrj.cr.24-0005
中图分类号
R61 [外科手术学];
学科分类号
摘要
INTRODUCTION: A pneumatocele is a cystic change in the lung that can develop as a sequelae of infection, inflammation, positive-pressure ventilation, thoracic trauma, and rarely after lung resection. Pneumatocele development triggered by an extrathoracic etiology is rare. Herein, we report a case of a pneumatocele that developed after a deceased-donor liver transplantation. CASE PRESENTATION: A 57-year-old woman with a diagnosis of autosomal dominant polycystic kidney disease underwent deceased-donor liver transplantation for polycystic liver disease. She did not have any background lung disease, although her right lower lobe was mostly atelectatic due to a remarkably elevated diaphragm. The liver transplant itself was uneventful. A small hole was made in the right diaphragm during the dissection of the liver, but it was successfully repaired without any injury to the lung. On postoperative day 1, the chest radiograph revealed a round hypertranslucency on the right side, which was initially considered subphrenic air retention, and no further evaluation was made at that time. Given that the hypertranslucency persisted, follow-up computed tomography was performed on postoperative day 18, and revealed an air-fluid level above the diaphragm in the right thoracic cavity. Thoracoscopic investigation revealed an intrathoracic hematoma within a pneumatocele in the right lower lobe, which was not detected in the pretransplant computed tomography. The hematoma was removed, and the pneumatocele was resected. CONCLUSIONS: We experienced a case of a pneumatocele that developed after deceased-donor liver transplantation for multiple hepatic cysts due to autosomal dominant polycystic kidney disease. Although the mechanisms are speculative, the pneumatocele might have been triggered by the sudden alleviation of the elevated diaphragm and reinflation of the atelectatic lung.
引用
收藏
页数:6
相关论文
共 50 条
  • [21] Congenital Hepatic Fibrosis in a Case of Autosomal Dominant Polycystic Kidney Disease: A Case Report
    Majethia, Nikhil
    Haria, Pankti
    Patel, R. D.
    Gadgil, Nitin
    Kalgutkar, Alka
    INTERNATIONAL JOURNAL OF SCIENTIFIC STUDY, 2014, 2 (08) : 243 - 245
  • [22] RISK-FACTORS FOR THE DEVELOPMENT OF HEPATIC CYSTS IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE
    GABOW, PA
    JOHNSON, AM
    KAEHNY, WD
    MANCOJOHNSON, ML
    DULEY, IT
    EVERSON, GT
    HEPATOLOGY, 1990, 11 (06) : 1033 - 1037
  • [23] The Longitudinal Study of Liver Cysts in Patients With Autosomal Dominant Polycystic Kidney Disease and Polycystic Liver Disease
    Matsuura, Ryo
    Honda, Kenjiro
    Hamasaki, Yoshifumi
    Doi, Kent
    Noiri, Eisei
    Nangaku, Masaomi
    KIDNEY INTERNATIONAL REPORTS, 2017, 2 (01): : 60 - 65
  • [24] CHARACTERISTICS OF HEPATIC CYSTS IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD)
    EVERSON, GT
    LEFF, N
    BROWN, WR
    EMMETT, M
    HEPATOLOGY, 1988, 8 (05) : 1341 - 1341
  • [25] Polycystic Liver and Kidney Volume Changes in Patients with Autosomal Dominant Polycystic Kidney Disease after Renal Transplantation
    Yamamoto, T.
    Watrai, Y.
    Kobayashi, T.
    Matsuda, Y.
    Tsujita, M.
    Hiramitsu, T.
    Nanmoku, K.
    Goto, N.
    Uchida, K.
    AMERICAN JOURNAL OF TRANSPLANTATION, 2012, 12 : 379 - 379
  • [26] Case report: Rare genetic liver disease - a case of congenital hepatic fibrosis in adults with autosomal dominant polycystic kidney disease
    Liu, Ying
    Zhu, Ping
    Tian, Jiajun
    FRONTIERS IN MEDICINE, 2024, 11
  • [27] Liver or Combined Liver-Kidney Transplantation for Autosomal Dominant Polycystic Kidney Disease
    D'Amico, Giuseppe
    Di Benedetto, Fabrizio
    Tarantino, Giuseppe
    De Ruvo, Nicola
    Cautero, Nicola
    Montalti, Roberto
    Guerrini, Gian Piero
    Ballarin, Roberto
    Spaggiari, Mario
    Baisi, Beniamino
    Cappelli, Gianni
    Gerunda, Giorgio E.
    LIVER TRANSPLANTATION, 2011, 17 (06) : S282 - S282
  • [28] Liver or Combined Liver-Kidney Transplantation for Autosomal Dominant Polycystic Kidney Disease
    Di Benedetto, Fabrizio
    D'Amico, Giuseppe
    De Ruvo, Nicola
    Montalti, Roberto
    Cautero, Nicola
    Guerrini, Gian Piero
    Ballarin, Roberto
    Spaggiari, Mario
    Iemmolo, Rosa Maria
    Marino, Maria
    Smerieri, Nazareno
    Mimmo, Antonio
    Bianchi, Gian Paolo
    Gerunda, Giorgio E.
    LIVER TRANSPLANTATION, 2010, 16 (06) : S242 - S243
  • [29] Spiny keratoderma in association with autosomal dominant polycystic kidney disease with liver cysts
    Anderson, D
    Cohen, DE
    Lee, HS
    Thellman, C
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1996, 34 (05) : 935 - 936
  • [30] A successful case of deceased-donor liver transplantation from a donor with Marfan syndrome: a case report
    Takuma Ishikawa
    Shinji Itoh
    Takeo Toshima
    Yuki Nakayama
    Katsuya Toshida
    Yuriko Tsutsui
    Norifumi Iseda
    Takuma Izumi
    Shohei Yoshiya
    Mizuki Ninomiya
    Tomoharu Yoshizumi
    Surgical Case Reports, 10