Teratoma of the hepatic hilum. Report of a rare case

Grażyna Poniatowska-Broniek; Tomasz Siwko; Magdalena Misiukiewicz-Poć; Wojciech Choiński; Marian Sulik

doi:10.1016/j.poamed.2014.04.003

1/2014 vol. 21

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CASE REPORT

Teratoma of the hepatic hilum. Report of a rare case

Grażyna Poniatowska-Broniek ^{1, 2}

, Tomasz Siwko ¹, Magdalena Misiukiewicz-Poć ², Wojciech Choiński ³, Marian Sulik ²

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1	Department of Pathomorphology, Regional Children's Specialist Hospital in Olsztyn, Poland
2	Department of Pathology, Faculty of Medical Science, University of Warmia and Mazury in Olsztyn, Poland
3	Department of Pediatric Surgery, Regional Children's Specialist Hospital in Olsztyn, Poland

CORRESPONDING AUTHOR

Grażyna Poniatowska-Broniek

Department of Pathomorphology, Regional Children's Specialist Hospital in Olsztyn, Żołnierska 18 a, 10-561 Olsztyn, Poland. Tel.: +48 89 539 32 97.

Submission date: 2013-12-04

Acceptance date: 2014-04-15

Online publication date: 2014-05-15

Publication date: 2020-03-26

Pol. Ann. Med. 2014;21(1):40–44

DOI: https://doi.org/10.1016/j.poamed.2014.04.003

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References (14)

KEYWORDS

ABSTRACT

Introduction:
Teratoma is a rarely occurring neoplasm characterized by an abnormal growth of tissues deriving from three germinal layers: endoderm, mesoderm and ectoderm. Liver is a very rare site for teratoma, as only 28 hepatic teratomas were reported, including 21 in children. Furthermore, teratoma of the liver accounts for less than 1% of all hepatic neoplasms and the majority of these cases occurred in female children below the age of three. Hence, our case is particularly unique.

Aim:
The aim of this paper was to report a rare case of a teratoma of the hepatic hilum.

Case study:
We report a case of a 12-year-old boy suffering from abdominal pain since the age of 2. Medical imaging revealed an abdominal cyst and after the surgery and histological examination mature teratoma of the hepatic hilum was diagnosed.

Results and discussion:
Hilum is particularly unique localization for a liver teratoma, as so far only one such case has been reported. The histology showed a mixture of mature tissues, and no immature elements were found. Thus, histology was typical for Teratoma maturum.

Conclusions:
The case described here represent a rare case of hepatic teratoma with particularly unique localization in the hepatic hilum.

CONFLICT OF INTEREST

None declared.

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