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A Glomus Tumor Presenting on the Ventromedial Aspect of the Little Finger Causing Bony Erosion: A Rare Case From India.
Solunke, Swaroop; Gundecha, Pratik T; Gupta, Archit; Salunkhe, Rahul; Nair, Abhishek.
Afiliação
  • Solunke S; Orthopaedics, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Pune, IND.
  • Gundecha PT; Orthopaedic Surgery, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Pune, IND.
  • Gupta A; Orthopaedics, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Pune, IND.
  • Salunkhe R; Orthopaedics, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Pune, IND.
  • Nair A; Orthopaedics, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Pune, IND.
Cureus ; 16(2): e54173, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38496094
ABSTRACT
Glomus tumors are rare neoplasms originating from the glomus body that predominantly manifest in the subungual region of the digits and are distinguished by severe pain and a heightened sensitivity to cold. Bony erosion associated with glomus tumors is a rare phenomenon. Here, we present a unique case of a glomus tumor situated on the ventromedial aspect of the little finger, leading to notable bony erosion. A 42-year-old female from India presented with a chief complaint of severe and localized pain in the ventromedial region of her right little finger, exacerbated by exposure to cold temperatures. Radiological investigations demonstrated focal bone erosion at the site of the tumor. Surgical excision of the lesion was performed. A fish-mouth incision was made on the ventromedial aspect of the little finger, which was extended to the tip of the finger. The nail bed was kept intact. The tumor was excised using small forceps. The patient experienced complete resolution of symptoms postoperatively and reported no recurrence during the follow-up period. This case report highlights the exceptional presentation of a glomus tumor causing bony erosion on the ventromedial aspect of the little finger, a manifestation rarely encountered in clinical practice. Furthermore, this case contributes to the limited body of literature on this combination of uncommon clinical entities, shedding light on its diagnosis and management.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos