Observational case report.
To report a case of dorsal cutaneous appendage or the so-called human tail that was the cause of tethered cord syndrome.
The dorsal cutaneous appendage, or so-called human tail, is often considered to be a cutaneous marker of underlying occult spinal dysraphism. In such cases, there is usually a separate underlying tethering lesion. There have been only three case reports in the literature where this appendage itself was the tethering lesion. The fourth such case is being reported.
An 11-month-old male child was brought for consultation for a “tail-like” structure in the low back since birth. Examination revealed a subtle thinning of the right lower extremity and a caudal appendage in the lower lumbar region. Plain radiographs revealed spina bifida at S1. MRI revealed a transitional lipoma at L5–S1 with a terminal syrinx.
During surgery, a fibrous tract was seen extending from the base of the appendage through the defect in the bone and dura. The tract ended in the transitional lipoma of the cord at L5–S1. Sectioning of the tract and debulking of the transitional lipoma was done. After surgery, there was no change in the neurologic status of the patient.
This case illustrates that the so-called “human tail” or the dorsal cutaneous appendage is not just a marker of underlying occult spinal dysraphism. In rare cases, the appendage itself can be the tethering lesion. In every case of dorsal cutaneous appendage, the surgeon should diligently search for the intraspinal extension of the lesion even if such an extension is not revealed by the MRI.
The dorsal cutaneous appendage or the so-called “human tail” is often considered to be a cutaneous marker of occult spinal dysraphism. In rare instances, this appendage itself can be a cause of tethering. Therefore, in every case of dorsal cutaneous appendage, the surgeon should diligently search for an intraspinal extension.
From the Department of Neurosurgery, Madurai Medical College, Madurai, India.
Acknowledgment date: December 23, 2003. Acceptance date: January 5, 2004.
The manuscript submitted does not contain information about medical device(s)/drug(s).
No funds were received in support of this work. No benefits in any form have been or will be received from a commercial party related directly or indirectly to the subject of this manuscript.
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