APHALLIA: A VERY RARE CONGENITAL ANOMALY, WITH ASSOCIATED GENITOURINARY AND ANO-RECTAL MALFORMATION

Authors

  • Muhammad Umar Nisar Children Hospital Pakistan Institute Of Medical Sciences Islamabad
  • Nadeem Akhtar Children Hospital Pakistan Institute Of Medical Sciences Islamabad
  • Mudassar Fiaz Gondal Children Hospital Pakistan Institute Of Medical Sciences Islamabad
  • Samer Sikander PAEC General Hospital PIMS
  • Sana Viqar rawalpindi medical college

Abstract

Aphallia or penile agenesis is very rare congenital anomaly of unknown cause occurring 1 in 30 million live births. Very little has been written in literature about aphallia. There is absent phallus and urethra may open abnormally in perineum or into rectum posing various surgical, social and psychological implications as the child grows.  We are presenting 03 cases of aphallia with associated congenital anomalies such as unilateral renal agenesis, bilateral undescended testes, anorectal malformation and rectovasical fistula.

Keywords: Aphallia; Penile agenesis; Absent penis; Ambiguous genetalia; Phalloplasty; Neo-phallus; Penile reconstruction

Author Biographies

Muhammad Umar Nisar, Children Hospital Pakistan Institute Of Medical Sciences Islamabad

Resident Pediatric Surgery 

Children Hospital
Pakistan Institute Of Medical Sciences
Islamabad

 

Nadeem Akhtar, Children Hospital Pakistan Institute Of Medical Sciences Islamabad

Professor & Head of department pediatric Surgery

Children Hospital, PIMS, Islamabad 

Mudassar Fiaz Gondal, Children Hospital Pakistan Institute Of Medical Sciences Islamabad

assistant professor 

pediatric surgery 

children hospital , PIMS 

islamabad

Samer Sikander, PAEC General Hospital PIMS

resident pediatrics 

 

Sana Viqar, rawalpindi medical college

MBBS FINAL YEAR

References

Demirer Z, Aip B, Uguz S, Guragac A, Irkilata H. A rare case of penis agenesis (Aphallia) with associated multiple urogenital anomalies. Int J Surg Case Rep 2015;15:10-12.

Bangroo AK, Khetri R, Tiwari S. Penile agenesis. J Indian Assoc Pediatr Surg 2005;10(4):256-7.

Mirshemirani A, Khaleghnejad A, Pourang H, Sadeghian N, Rouzrokh M, Salehpour S. Penile agenesis: report on 8 cases and review of literature. Iran J Pediatr 2009;19(2):173-9.

Aslanabadi S, Zarrintan S, Abdollahi H, Rikhtegar R, Beheshtirouy S, Badebarin D, et al. A Rare Case of Aphallia with Right Kidney Hypoplasia and Left Kidney Dysplasia. Arch Iran Med 2015;18(4):257-9.

Sharma D, Singh R, Shastri R. A case report of aphallia with urorectal septum malformation sequence in a newborn: a very rarely seen condition. Int Med Case Rep J 2015;8:317-20.

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Published

2018-03-16

How to Cite

Nisar, M. U., Akhtar, N., Gondal, M. F., Sikander, S., & Viqar, S. (2018). APHALLIA: A VERY RARE CONGENITAL ANOMALY, WITH ASSOCIATED GENITOURINARY AND ANO-RECTAL MALFORMATION. Journal of Ayub Medical College Abbottabad, 30(2), 275–277. Retrieved from https://jamc.ayubmed.edu.pk/index.php/jamc/article/view/3528

Issue

Vol. 30 No. 2 (2018): JOURNAL OF AYUB MEDICAL COLLEGE, ABBOTTABAD

Section

CASE SERIES

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