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Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis

BACKGROUND: Fetus in fetu (FIF) is a rare entity in which a malformed diamniotic monochorionic parasitic fetal twin develops inside a normal co-twin’s body, most commonly in the abdominal cavity. FIF is differentiated from the teratoma by the presence of vertebral column often with an appropriate ar...

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Autores principales: Sitharama, Suhas Aithal, Jindal, Bibekanand, Vuriti, Mrudula Kumari, Naredi, Bikash Kumar, Krishnamurthy, Sriram, Subramania, Deepak Barathi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295181/
https://www.ncbi.nlm.nih.gov/pubmed/28217238
http://dx.doi.org/10.12659/PJR.899956
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author Sitharama, Suhas Aithal
Jindal, Bibekanand
Vuriti, Mrudula Kumari
Naredi, Bikash Kumar
Krishnamurthy, Sriram
Subramania, Deepak Barathi
author_facet Sitharama, Suhas Aithal
Jindal, Bibekanand
Vuriti, Mrudula Kumari
Naredi, Bikash Kumar
Krishnamurthy, Sriram
Subramania, Deepak Barathi
author_sort Sitharama, Suhas Aithal
collection PubMed
description BACKGROUND: Fetus in fetu (FIF) is a rare entity in which a malformed diamniotic monochorionic parasitic fetal twin develops inside a normal co-twin’s body, most commonly in the abdominal cavity. FIF is differentiated from the teratoma by the presence of vertebral column often with an appropriate arrangement of other organs or limbs around it. CASE REPORT: A two-and-a-half-year-old girl presented with a painless abdominal swelling in the right hypochondrium. On imaging, a heterogenous soft tissue mass with internal calcific densities was noted in the retroperitoneum. The mass had vertebral organization, limb and pelvic bones. The presence of a fetiform teratoma was suspected and surgery revealed an encapsulated mass with an anencephalic head, spine, upper and lower limb buds. Histopathology confirmed the presence of a fetus in fetu. The postoperative period was uneventful with no evidence of recurrence. CONCLUSIONS: FIF is a pediatric rarity. Cross-sectional imaging helps in differentiating it from a teratoma, meconium peritonitis and abdominal ectopic pregnancy. Surgical excision is the treatment of choice for this benign condition, which requires a follow-up only in certain cases. This case report describes a retroperitoneal fetus in fetu and discusses its clinical presentation, differential diagnosis and embryologic origin.
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spelling pubmed-52951812017-02-17 Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis Sitharama, Suhas Aithal Jindal, Bibekanand Vuriti, Mrudula Kumari Naredi, Bikash Kumar Krishnamurthy, Sriram Subramania, Deepak Barathi Pol J Radiol Case Report BACKGROUND: Fetus in fetu (FIF) is a rare entity in which a malformed diamniotic monochorionic parasitic fetal twin develops inside a normal co-twin’s body, most commonly in the abdominal cavity. FIF is differentiated from the teratoma by the presence of vertebral column often with an appropriate arrangement of other organs or limbs around it. CASE REPORT: A two-and-a-half-year-old girl presented with a painless abdominal swelling in the right hypochondrium. On imaging, a heterogenous soft tissue mass with internal calcific densities was noted in the retroperitoneum. The mass had vertebral organization, limb and pelvic bones. The presence of a fetiform teratoma was suspected and surgery revealed an encapsulated mass with an anencephalic head, spine, upper and lower limb buds. Histopathology confirmed the presence of a fetus in fetu. The postoperative period was uneventful with no evidence of recurrence. CONCLUSIONS: FIF is a pediatric rarity. Cross-sectional imaging helps in differentiating it from a teratoma, meconium peritonitis and abdominal ectopic pregnancy. Surgical excision is the treatment of choice for this benign condition, which requires a follow-up only in certain cases. This case report describes a retroperitoneal fetus in fetu and discusses its clinical presentation, differential diagnosis and embryologic origin. International Scientific Literature, Inc. 2017-01-30 /pmc/articles/PMC5295181/ /pubmed/28217238 http://dx.doi.org/10.12659/PJR.899956 Text en © Pol J Radiol, 2017 This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.
spellingShingle Case Report
Sitharama, Suhas Aithal
Jindal, Bibekanand
Vuriti, Mrudula Kumari
Naredi, Bikash Kumar
Krishnamurthy, Sriram
Subramania, Deepak Barathi
Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis
title Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis
title_full Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis
title_fullStr Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis
title_full_unstemmed Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis
title_short Fetus in Fetu: Case Report and Brief Review of Literature on Embryologic Origin, Clinical Presentation, Imaging and Differential Diagnosis
title_sort fetus in fetu: case report and brief review of literature on embryologic origin, clinical presentation, imaging and differential diagnosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295181/
https://www.ncbi.nlm.nih.gov/pubmed/28217238
http://dx.doi.org/10.12659/PJR.899956
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