Hepatocellular Carcinoma With Situs Inversus Totalis-a Case Report-

Iwakura, Shinji; Nakai, Takehiro; Hirokawa, Fumitoshi

doi:10.3919/jjsa.59.3100

Cited by 2 publications

(2 citation statements)

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“…To our knowledge, this is the first report of isolated caudate lobectomy in a patient with SIT. Including the present case, 6 of 14 reports in which anatomy of hepatic artery were described showed variations in hepatic artery [3] , [4] , [5] , [6] , [7] , [8] , [9] , [10] , [11] , [12] , [13] , [14] , [15] . These factors suggest that in patients with SIT, not only the mirror-image relationship of the organs to the normal condition, but also the anatomical variations of the vascular system, including the hepatic arteries, increase the difficulty of surgical procedures.…”

Section: Discussionmentioning

confidence: 57%

“…lobe 14 ∗ 12 cm Rt. lobectomy RHA arising from SMA 3 1996 Kamiike [5] 69/F LC Combined S7 2.5 cm Resection of postero-superior segment None 4 1998 Iwakura [6] 63/M LC-C HCC S6 1.5 cm Lower posterior segmentectomy None 5 1998 Hamada [7] 60/F LC-C HCC S6-7 2.5 cm Partial resection None 6 1999 Seshimo [8] 70/M LC-C HCC Lat. seg.…”

Section: Discussionmentioning

confidence: 99%

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Hepatocellular carcinoma with situs inversus totalis treated by caudate lobectomy: A case report

Kitasato

Miyoshi

Okamoto

et al. 2022

International Journal of Surgery Case Reports

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Section: Discussionmentioning

confidence: 57%

Section: Discussionmentioning

confidence: 99%

Hepatocellular carcinoma with situs inversus totalis treated by caudate lobectomy: A case report

Kitasato

Miyoshi

Okamoto

et al. 2022

International Journal of Surgery Case Reports

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Situs Inversus Totalis (SIT) with Hepatocellular Carcinoma (HCC): A Rare Case Report and Review of 12 Other Cases

et al. 2012

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Hepatocellular carcinoma (HCC) is the seventhmost common malignancy in males and ninth in females with incidence of one million new cases every year. Situs inversus totalis (SIT) is a rare congenital condition, in which there is a mirror-image transposition of both the abdominal and thoracic viscera. There are very few reported cases of HCC developing in people with SIT. In this review, we present a new case of HCC with SIT, and a review of literatures published between 1983 and 2011 on it. The literatures in English were searched through PubMed and Google Scholar, while those in Japanese language were accessed through J-EAST and translated in English with the help of Google translator on 22 April 2012. There are 6 English and 6 Japanese literatures showing 12 published cases, of which 10 cases were from Japan, 1 from Taiwan and 1 from China. Our case is probably the first case in the world beyond these regions. The articles containing adequate information, such as patient age and sex, investigations, diagnosis, type of congenital anomalies and methods of surgery, were reviewed. On reviewing the literature, we observed that clinical manifestations, laboratory findings and etiology correlate well with HCC, while anomalous hepatic vascularity correlates well with SIT. The reason for high incidence of HCC with SIT in Japan is not well correlated, but may be explained by higher incidence of SIT. All varieties of hepatic resection were feasible in cases of SIT.

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Hepatocellular Carcinoma With Situs Inversus Totalis-a Case Report-

Cited by 2 publications

References 3 publications

Hepatocellular carcinoma with situs inversus totalis treated by caudate lobectomy: A case report

Hepatocellular carcinoma with situs inversus totalis treated by caudate lobectomy: A case report

Situs Inversus Totalis (SIT) with Hepatocellular Carcinoma (HCC): A Rare Case Report and Review of 12 Other Cases

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