TY - JOUR
T1 - Colon perforation due to antigenemia-negative cytomegalovirus gastroenteritis after liver transplantation
T2 - A case report and review of literature
AU - Yokose, Takahiro
AU - Obara, Hideaki
AU - Shinoda, Masahiro
AU - Nakano, Yutaka
AU - Kitago, Minoru
AU - Yagi, Hiroshi
AU - Abe, Yuta
AU - Yamada, Yohei
AU - Matsubara, Kentaro
AU - Oshima, Go
AU - Hori, Shutaro
AU - Ibuki, Sho
AU - Higashi, Hisanobu
AU - Masuda, Yuki
AU - Hayashi, Masanori
AU - Mori, Takehiko
AU - Kawaida, Miho
AU - Fujimura, Takumi
AU - Hoshino, Ken
AU - Kameyama, Kaori
AU - Kuroda, Tatsuo
AU - Kitagawa, Yuko
N1 - Publisher Copyright:
© The Author(s) 2019.
PY - 2019
Y1 - 2019
N2 - BACKGROUND Cytomegalovirus (CMV) remains a critical complication after solid-organ transplantation. The CMV antigenemia (AG) test is useful for monitoring CMV infection. Although the AG-positivity rate in CMV gastroenteritis is known to be low at onset, almost all cases become positive during the disease course. We treated a patient with transverse colon perforation due to AG-negative CMV gastroenteritis, following a living donor liver transplantation (LDLT). CASE SUMMARY The patient was a 52-year-old woman with decompensated liver cirrhosis as a result of autoimmune hepatitis who underwent a blood-type compatible LDLT with her second son as the donor. On day 20 after surgery, upper and lower gastrointestinal endoscopy (GE) revealed multiple gastric ulcers and transverse colon ulcers. The biopsy tissue immunostaining confirmed a diagnosis of CMV gastroenteritis. On day 28 after surgery, an abdominal computed tomography revealed transverse colon perforation, and simple lavage and drainage were performed along with an urgent ileostomy. Although the repeated remission and aggravation of CMV gastroenteritis and acute cellular rejection made the control of immunosuppression difficult, the upper GE eventually revealed an improvement in the gastric ulcers, and the biopsy samples were negative for CMV. The CMV-AG test remained negative, therefore, we had to evaluate the status of the CMV infection on the basis of the clinical symptoms and GE. CONCLUSION This case report suggests a monitoring method that could be useful for AG-negative CMV gastroenteritis after a solid-organ transplantation.
AB - BACKGROUND Cytomegalovirus (CMV) remains a critical complication after solid-organ transplantation. The CMV antigenemia (AG) test is useful for monitoring CMV infection. Although the AG-positivity rate in CMV gastroenteritis is known to be low at onset, almost all cases become positive during the disease course. We treated a patient with transverse colon perforation due to AG-negative CMV gastroenteritis, following a living donor liver transplantation (LDLT). CASE SUMMARY The patient was a 52-year-old woman with decompensated liver cirrhosis as a result of autoimmune hepatitis who underwent a blood-type compatible LDLT with her second son as the donor. On day 20 after surgery, upper and lower gastrointestinal endoscopy (GE) revealed multiple gastric ulcers and transverse colon ulcers. The biopsy tissue immunostaining confirmed a diagnosis of CMV gastroenteritis. On day 28 after surgery, an abdominal computed tomography revealed transverse colon perforation, and simple lavage and drainage were performed along with an urgent ileostomy. Although the repeated remission and aggravation of CMV gastroenteritis and acute cellular rejection made the control of immunosuppression difficult, the upper GE eventually revealed an improvement in the gastric ulcers, and the biopsy samples were negative for CMV. The CMV-AG test remained negative, therefore, we had to evaluate the status of the CMV infection on the basis of the clinical symptoms and GE. CONCLUSION This case report suggests a monitoring method that could be useful for AG-negative CMV gastroenteritis after a solid-organ transplantation.
KW - Antigenemia negative
KW - Case report
KW - Colon perforation
KW - Cytomegalovirus gastrointestinal disease
KW - Liver transplantation
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U2 - 10.3748/wjg.v25.i15.1899
DO - 10.3748/wjg.v25.i15.1899
M3 - Article
C2 - 31057303
AN - SCOPUS:85065259608
SN - 1007-9327
VL - 25
SP - 1899
EP - 1906
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 15
ER -