Ultrasound-Guided Hook-Wire Localization for Excision of Non-palpable Cervical Lesions Suspicious for Metastasis
The goal of this randomized controlled trial is to determine whether ultrasound-guided hook-wire localization improves surgical efficiency and accuracy compared with ultrasound-guided surgery alone for the excision of non-palpable or difficult-to-palpate cervical lesions suspicious for metastatic disease in adult patients.
The main questions it aims to answer are:
* Does ultrasound-guided hook-wire localization reduce operative time compared with ultrasound-guided excision alone?
* Does hook-wire localization improve surgical precision, including successful retrieval of the target lesion for histopathological assessment?
* Does hook-wire localization affect incision length, procedural difficulty, or the risk of surgical complications?
Researchers will compare patients undergoing ultrasound-guided hook-wire localization followed by surgical excision with patients undergoing ultrasound-guided excision alone to determine whether hook-wire guidance improves surgical outcomes.
Participants will:
* Undergo ultrasound-guided localization and surgical excision of a cervical lesion or lymph node suspicious for malignancy.
* Be randomly assigned to either: ultrasound-guided hook-wire localization before surgery, or ultrasound-guided excision without hook-wire localization.
* Have surgical outcomes assessed, including operative time, incision length, successful lesion retrieval, procedural difficulty, and intraoperative or postoperative complications.
Gender: All
Ages: 18 Years - Any
Non Palpable Cervical Lesions Suspicious for Metastasis