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Axillary synovial sarcoma recurrence involving brachial plexus, a rare case report from Pakistan.
Virji, Safna Naozer; Pirzada, Muhammad Ammar; Siddiqui, Nadeem Ahmed; Idrees, Romana; Zeeshan, Sana.
Afiliação
  • Virji SN; Section of General Surgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan. Electronic address: safna.virji@aku.edu.
  • Pirzada MA; Section of Vascular Surgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan.
  • Siddiqui NA; Section of Vascular Surgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan. Electronic address: nadeem.siddiqui@aku.edu.
  • Idrees R; Pathology and Laboratory Medicine, Aga Khan University Hospital, Karachi, Pakistan. Electronic address: romana.idress@aku.edu.
  • Zeeshan S; Section of Breast Surgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan. Electronic address: sana.zeeshan@aku.edu.
Int J Surg Case Rep ; 107: 108325, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37224725
ABSTRACT

INTRODUCTION:

Synovial sarcomas are rare tumors, and the incidence of axillary synovial sarcoma involving the brachial plexus has been reported as 2.9 % among all axillary soft tissue tumors. However, the recurrence of axillary synovial sarcomas has not been reported in literature. CASE PRESENTATION A 36-years-old Afghan female presented in Karachi, Pakistan with a history of persistently increasing, recurrent, right axillary mass for 6 months. Initially diagnosed as a spindle-cell tumor on excision in Afghanistan, she had received ifosfamide and doxorubicin, but the lesion recurred. On examination, it was a 5 × 6 cm, hard mass palpable in right axilla. After radiological work-up and a multidisciplinary team discussion, she underwent complete excision of the tumor with successful preservation of brachial plexus. The final diagnosis was reported as monophasic synovial sarcoma FNCLCC Grade 3.

DISCUSSION:

Our patient presented with a recurrent right axillary synovial sarcoma that was involving the axillary neurovascular bundle and brachial plexus, which was initially diagnosed as a spindle cell sarcoma. Pre-operative core-needle biopsy was unable to provide a definitive diagnosis. MRI scan was useful in delineating the proximity of the neurovascular structures. Re-excision of the tumor was performed which is the mainstay of treatment for axillary synovial sarcomas, combined with radiotherapy depending on the disease grading, staging and patient factors.

CONCLUSION:

Axillary synovial sarcoma recurrence with involvement of the brachial plexus is an extremely rare presentation. Our patient was successfully managed through a multidisciplinary approach with complete surgical excision and preservation of the brachial plexus followed by adjuvant radiotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2023 Tipo de documento: Article