Skip to main content
Top
Published in: BMC Musculoskeletal Disorders 1/2020

Open Access 01-12-2020 | Carpal Tunnel Syndrome | Case report

Atypical osteochondroma of the hamate that presented clinically as carpal tunnel syndrome: report of an extremely rare case and literature review

Authors: Makoto Motomiya, Taiki Sakazaki, Norimasa Iwasaki

Published in: BMC Musculoskeletal Disorders | Issue 1/2020

Login to get access

Abstract

Background

Osteochondroma is a benign tumor that occurs mainly at the metaphysis of long bones and seldom arises from carpal bones. We describe an extremely rare case of osteochondroma of the hamate without a typical cartilaginous cap and with a spiky bony protrusion in an elderly patient.

Case presentation

A 78-year-old right-handed female housekeeper had a multilobed osteochondroma of the hamate, which caused carpal tunnel syndrome and irritation of the flexor tendons. Radiological examinations showed a morphological abnormality of the hamate comprising a spiky bony protrusion into the carpal tunnel and a free body proximal to the pisiform. Open carpal tunnel release and resection of the spiky bony protrusion on the hook of the hamate were performed. The flexor digitorum profundus tendons of the ring and little fingers displayed synovitis and partial laceration in the carpal tunnel. Histological examination also showed atypical findings: only a few regions of cartilaginous tissue were seen in the spiky bony protrusion, whereas the free body proximal to the pisiform contained thick cartilaginous tissue such as a cartilaginous cap typical of osteochondroma. We speculated that the bony protrusion to the carpal tunnel had been eroded by mechanical irritation caused by gliding of the flexor tendon and had resulted in the protruding spiky shape with less cartilaginous tissue. The fractured cartilaginous cap had moved into the cavity within the carpal tunnel proximal to the pisiform and had become a large free body.

Conclusions

Osteochondroma of the carpal bone may take various shapes because the carpal bone is surrounded by neighboring bones and tight ligaments, which can restrict tumor growth. This type of tumor is likely to present with various symptoms because of the close proximity of important structures including nerves, tendons, and joints. The diagnosis of osteochondroma of the carpal bone may be difficult because of its rarity and atypical radiological and histological findings, such as the lack of a round cartilaginous cap. We suggest that surgeons should have a detailed understanding of this condition and should make a definitive diagnosis based on the overall findings.
Literature
1.
go back to reference Murphey MD, Choi JJ, Kransdorf MJ, Flemming DJ, Gannon FH. Imaging of osteochondroma: variants and complications with radiologic-pathologic correlation. Radiographics. 2000;20:1407–34.CrossRef Murphey MD, Choi JJ, Kransdorf MJ, Flemming DJ, Gannon FH. Imaging of osteochondroma: variants and complications with radiologic-pathologic correlation. Radiographics. 2000;20:1407–34.CrossRef
2.
go back to reference Katayama T, Ono H, Furuta K. Osteochondroma of the lunate with extensor tendons rupture of the index finger: a case report. J Hand Surg Asian Pac Vol. 2011;16:181–4. Katayama T, Ono H, Furuta K. Osteochondroma of the lunate with extensor tendons rupture of the index finger: a case report. J Hand Surg Asian Pac Vol. 2011;16:181–4.
3.
go back to reference Uchida K, Kobayashi S, Takamura T, Yayama T, Inukai T, Baba H. Osteochondroma arising from the scaphoid. J Orthop Sci. 2007;12:381–4.CrossRef Uchida K, Kobayashi S, Takamura T, Yayama T, Inukai T, Baba H. Osteochondroma arising from the scaphoid. J Orthop Sci. 2007;12:381–4.CrossRef
4.
go back to reference Cha SM, Shin HD, Kim DY. A solitary unilobed osteochondroma of the hamate: a case report. J Pediatr Orthop B. 2017;26:274–6.CrossRef Cha SM, Shin HD, Kim DY. A solitary unilobed osteochondroma of the hamate: a case report. J Pediatr Orthop B. 2017;26:274–6.CrossRef
5.
go back to reference Koti M, Honakeri SP, Thomas A. A multilobed osteochondroma of the hamate: case report. J Hand Surg Am. 2009;34:1515–7.CrossRef Koti M, Honakeri SP, Thomas A. A multilobed osteochondroma of the hamate: case report. J Hand Surg Am. 2009;34:1515–7.CrossRef
6.
go back to reference Shah NR, Wilczynski M, Gelberman R. Osteochondroma of the capitate causing rupture of the extensor digiti minimi: case report. J Hand Surg [Am]. 2009;34:46–8.CrossRef Shah NR, Wilczynski M, Gelberman R. Osteochondroma of the capitate causing rupture of the extensor digiti minimi: case report. J Hand Surg [Am]. 2009;34:46–8.CrossRef
7.
go back to reference Carpintero P, Leon F, Zafra M, Montero M, Berral FJ. Fractures of osteochondroma during physical exercise. Am J Sports Med. 2003;31:1003–6.CrossRef Carpintero P, Leon F, Zafra M, Montero M, Berral FJ. Fractures of osteochondroma during physical exercise. Am J Sports Med. 2003;31:1003–6.CrossRef
8.
go back to reference Passanise AM, Mehlman CT, Wall EJ, Dieterle JP. Radiographic evidence of regression of a solitary osteochondroma: a report of 4 cases and a literature review. J Pediatr Orthop. 2011;31:312–6.CrossRef Passanise AM, Mehlman CT, Wall EJ, Dieterle JP. Radiographic evidence of regression of a solitary osteochondroma: a report of 4 cases and a literature review. J Pediatr Orthop. 2011;31:312–6.CrossRef
9.
go back to reference Takagi T, Matsumura T, Shiraishi T. Lunate osteochondroma: a case report. J Hand Surg [Am]. 2005;30:693–5.CrossRef Takagi T, Matsumura T, Shiraishi T. Lunate osteochondroma: a case report. J Hand Surg [Am]. 2005;30:693–5.CrossRef
10.
go back to reference Anantavorasakul N, Uerpairojkit C, Leechavengvongs S. Painful snapping of thumb caused by Osteochondroma of trapezium. J Hand Surg Asian Pac Vol. 2017;22:255–8.CrossRef Anantavorasakul N, Uerpairojkit C, Leechavengvongs S. Painful snapping of thumb caused by Osteochondroma of trapezium. J Hand Surg Asian Pac Vol. 2017;22:255–8.CrossRef
Metadata
Title
Atypical osteochondroma of the hamate that presented clinically as carpal tunnel syndrome: report of an extremely rare case and literature review
Authors
Makoto Motomiya
Taiki Sakazaki
Norimasa Iwasaki
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Musculoskeletal Disorders / Issue 1/2020
Electronic ISSN: 1471-2474
DOI
https://doi.org/10.1186/s12891-020-03272-8

Other articles of this Issue 1/2020

BMC Musculoskeletal Disorders 1/2020 Go to the issue