Spurious case of XX maleness in a patient with a history of Wiskott-Aldrich syndrome.

Abstract

OBJECTIVE:

To alert endocrinologists about the potential for karyotype confusion in patients who have undergone bone marrow transplantation.

METHODS:

Clinical, laboratory, and imaging data are reported on a young adult male patient who initially presented because of concerns about short stature.

RESULTS:

An 18-year-old fully virilized male patient with a history of Wiskott-Aldrich syndrome had undergone successful bone marrow transplantation in infancy. The donor was his older sister. Many years later, he underwent evaluation because of short stature and was found to have a 46, XX karyotype. This unexpected finding led to several costly laboratory and imaging studies, as well as a new diagnosis of a disorder of sex development. The patient was referred to our medical center for further evaluation of XX sex reversal. A skin biopsy was eventually performed, which revealed a 46, XY karyotype. This unusual case highlights the fact that a peripheral blood specimen from bone marrow transplant recipients reflects the genetic makeup of the bone marrow donor.

CONCLUSION:

Although the cytogenetic changes that occur in recipients of bone marrow transplants are well known to hematologists and oncologists, they are not commonly recognized by other health care providers. Increased awareness of this potential situation in long-term survivors of bone marrow transplantation is needed.

• Authors: Todd D Nebesio, Wilfredo Torres-Martinez, Richard C Rink, Erica A Eugster
• Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists (Endocr Pract) 2011 Mar-Apr Vol. 17 Issue 2 Pg. e1-3 ISSN: 1934-2403 [Electronic] United States
• PMID: 21041165 (Publication Type: Case Reports, Journal Article)

Topics

• Adolescent
• Bone Marrow Transplantation (adverse effects)
• Humans
• Karyotyping
• Male
• Ovotesticular Disorders of Sex Development (diagnosis, etiology, genetics)
• Wiskott-Aldrich Syndrome (therapy)