scholarly journals Fetus in fetu

2021 ◽  
Author(s):  
Mostafa El-Feky ◽  
Amany Gad
Keyword(s):  
2018 ◽  
Author(s):  
C Froehlich ◽  
A Woeckel ◽  
M Rehn ◽  
T Meyer
Keyword(s):  

2020 ◽  
Vol 22 ◽  
pp. 200450
Author(s):  
Mohammad Mosiur Rahman ◽  
Saumitra Chakravarty ◽  
Tani Barua
Keyword(s):  

2021 ◽  
Vol 69 (1) ◽  
Author(s):  
Moutaz Ragab ◽  
Omar Nagy Abdelhakeem ◽  
Omar Mansour ◽  
Mai Gad ◽  
Hesham Anwar Hussein

Abstract Background Fetus in fetu is a rare congenital anomaly. The exact etiology is unclear; one of the mostly accepted theories is the occurrence of an embryological insult occurring in a diamniotic monochorionic twin leading to asymmetrical division of the blastocyst mass. Commonly, they present in the infancy with clinical picture related to their mass effect. About 80% of cases are in the abdomen retroperitoneally. Case presentation We present two cases of this rare condition. The first case was for a 10-year-old girl that presented with anemia and abdominal mass, while the second case was for a 4-month-old boy that was diagnosed antenatally by ultrasound. Both cases had vertebrae, recognizable fetal organs, and skin coverage. Both had a distinct sac. The second case had a vascular connection with the host arising from the superior mesenteric artery. Both cases were intra-abdominal and showed normal levels of alpha-fetoprotein. Histopathological examination revealed elements from the three germ layers without any evidence of immature cells ruling out teratoma as a differential diagnosis. Conclusions Owing to its rarity, fetus in fetu requires a high degree of suspicion and meticulous surgical techniques to avoid either injury of the adjacent vital structures or bleeding from the main blood supply connection to the host. It should be differentiated from mature teratoma.


2013 ◽  
Vol 32 (12) ◽  
pp. 2212-2214 ◽  
Author(s):  
Recep Has ◽  
Ibrahim H. Kalelioglu ◽  
Aytul Corbacioglu Esmer ◽  
Reyhan Demirbas ◽  
Atil Yuksel ◽  
...  

1984 ◽  
Vol 82 (1) ◽  
pp. 115-119 ◽  
Author(s):  
Je G. Chi ◽  
Yoon S. Lee ◽  
Young Sik Park ◽  
Ka Yong Chang
Keyword(s):  

2006 ◽  
Vol 140A (16) ◽  
pp. 1737-1743 ◽  
Author(s):  
Shoko Miura ◽  
Kiyonori Miura ◽  
Toshiyuki Yamamoto ◽  
Michiko Yamanaka ◽  
Keisuke Saito ◽  
...  

1989 ◽  
Vol 24 (3) ◽  
pp. 296-299 ◽  
Author(s):  
Hock-Liew Eng ◽  
Jiin-Haur Chuang ◽  
Tze-Yu Lee ◽  
Wei-Jen Chen

2015 ◽  
pp. 80-83 ◽  
Author(s):  
Kristine KY Pang ◽  
◽  
Nicholas SY Chao ◽  
TK Tsang ◽  
Betty YT Lau ◽  
...  
Keyword(s):  

2021 ◽  
Vol 9 ◽  
Author(s):  
Mao Xiaowen ◽  
Cheng Lingxi ◽  
Lin Song ◽  
Pan Shengbao ◽  
Yang Xiaohong ◽  
...  

Objective: Fetus-in-fetu (FIF) is an extremely rare disease, and most prior publications are single case reports. Here, we describe the clinical characteristics, imaging manifestations, and the treatment and related complications of FIF from a large tertiary pediatric referral center.Materials: After institutional review board approval, patients with a diagnosis of FIF between January 2010 and November 2019 were further selected and reexamined. We analyzed the general clinical characteristics, imaging manifestations, treatment, and prognosis of the patients.Results: A total of seven (four male and three female) patients with FIF were included in the study. All patients were diagnosed with FIF during the antenatal ultrasound examination along with an abnormal increase in alpha fetoprotein, and it was confirmed by subsequent pathological examination. The median gestation period when FIF was first diagnosed was 25 (range: 22–32) weeks. Ultrasound, computed tomography, and magnetic resonance imaging were the main pre-operative diagnostic techniques used. All patients underwent FIF resection within 1 month after birth: four patients had open surgery and three had laparoscopic surgeries (one case was converted to open surgery); only one patient developed ascites after surgery. All patients are growing up healthy and without tumor recurrence at the last follow-up. The level of alpha fetoprotein decreased to normal within 1 year (range 3-10 months) after surgery performed.Conclusion: As the size of the FIF increases, it can be found and diagnosed in antenatal ultrasound examination. Surgery is an important curative treatment for FIF and generally results in excellent long-term quality of life.


1978 ◽  
Vol 13 (6) ◽  
pp. 771
Author(s):  
H. Suzuki
Keyword(s):  

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