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SACRAL syndrome.

Devendra Kumar Yadav1, Shasanka Shekhar Panda, Narinder Teckchandani

  • 1Department of Pediatric Surgery, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

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|August 2, 2013
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Summary
This summary is machine-generated.

Infantile haemangiomas are common benign tumors in infants. A rare case presented extensive superficial haemangioma from the neck to the perineum, accompanied by multiple congenital anomalies.

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Area of Science:

  • Pediatric Oncology
  • Dermatology
  • Neonatal Medicine

Background:

  • Haemangiomas are the most frequent tumors observed in infancy and early childhood.
  • These vascular tumors typically manifest within the first two weeks of a neonate's life.
  • While commonly affecting the head and neck, haemangiomas less frequently involve the lumbosacral and perineal regions.

Observation:

  • This report details an exceptionally rare case in a neonate.
  • The patient exhibited an extensive superficial haemangioma.
  • The anomaly spanned from the perineal region up to the neck, accompanied by multiple congenital anomalies.

Findings:

  • The case highlights an extremely rare presentation of infantile haemangioma.
  • Extensive cutaneous involvement from the perineum to the neck is highly unusual.
  • The co-occurrence of such extensive haemangioma with multiple congenital anomalies is exceedingly rare.

Implications:

  • This case underscores the importance of thorough examination in neonates with haemangiomas.
  • It emphasizes the potential for rare, widespread presentations and associated anomalies.
  • Further research into the etiology and management of extensive infantile haemangiomas with congenital anomalies is warranted.