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Chordoma arising from the coccygeal disc and mimicking a pilonidal cyst.
Mazzucco, Michael; Hwang, Sinchun; Linos, Konstantinos; Hameed, Meera; Shahzad, Farooq; Schmitt, Adam; Boland, Patrick; Vaynrub, Max.
Afiliación
  • Mazzucco M; Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, New York, NY, 10065, USA.
  • Hwang S; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
  • Linos K; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
  • Hameed M; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
  • Shahzad F; Plastic Surgery Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
  • Schmitt A; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
  • Boland P; Orthopaedic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.
  • Vaynrub M; Plastic Surgery Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. vaynrubm@mskcc.org.
Skeletal Radiol ; 2023 Nov 13.
Article en En | MEDLINE | ID: mdl-37953332
ABSTRACT
Chordomas are rare, low-grade malignant tumors often found in the sacrococcygeal region and prone to local recurrence. We report an atypical presentation of a 40-year-old patient with a symptomatic midline retrococcygeal lesion that was presumptively treated as a pilonidal cyst due to its clinical and imaging features. After surgical pathology rendered the diagnosis of chordoma, the patient required salvage surgery in the form of partial sacrectomy with soft tissue flap coverage. In addition to the unusually predominant retrococcygeal location, surgical pathology identified an intervertebral disc origin rather than the typical osseous origin. To our knowledge, this presentation of chordoma with coccygeal intervertebral origin and a large subcutaneous mass at imaging has rarely been reported in the literature. We describe this case to raise awareness of atypical presentations of sacrococcygeal chordoma that may lead to erroneous presumptive diagnosis and treatment.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Skeletal Radiol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Skeletal Radiol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos