Primary Cutaneous Adenoid Cystic Carcinoma Of The Chest Wall With Axillary Lymph Node Metastases And Its Management: A Case Report

Authors

  • Klein Dantis Assistant Professor, Department of Cardiothoracic Surgery, All India Institute of Medical Sciences, Raipur, India https://orcid.org/0000-0003-2348-2797
  • Radhakrishna Ramchandani Associate Professor, Department of General Surgery, All India Institute of Medical Sciences, Raipur, India https://orcid.org/0000-0002-6873-7805
  • Shamendra Anand Sahu Assistant Professor, Department of Burnsand Plastic Surgery, All India Institute of Medical Sciences, Raipur, India https://orcid.org/0000-0003-0877-8725
  • Vandita Yogendra Singh Associate Professor, Department of Pathology, All India Institute of Medical Sciences, Raipur, India https://orcid.org/0000-0003-1421-9700
  • Subhajit Dasgupta Junior resident, Department of Nuclear Medicine, All India Institute of Medical Sciences, Raipur, India

DOI:

https://doi.org/10.48729/pjctvs.293

Keywords:

Primary tumor, adenoid cystic, lymph node, chest wall, reconstruction

Abstract

Primary cutaneous adenoid cystic carcinoma (PCACC) is a rare form of adenoid cystic carcinoma (ACC) arising commonly from the salivary gland. Less often they originate outside the head and neck region, with the scalp being the commonest cutaneous site in 40% of the cases. The presentation on the chest wall is rare, with no reports to date on axillary lymph node metastases. Here we report a case of a 65-year-old female with previously operated PCACC of the chest wall at a different center, showing uptake on positron emission tomography imaging at the site of surgical scar that w as inconclusive on needle biopsy metastasized to the axillary lymph node confirmed by needle biopsy managed with wide local excision, axillary lymph node dissection, and chest wall reconstruction with keystone island flap. The postoperative outcome was uneventful with no recurrence or axillary complications at one year's follow-up. She was advised to receive adjuvant radiotherapy; however, she refused. To conclude, though PCACC is rare, they can have an aggressive presentation, and a multidisciplinary approach is necessary for a better outcome.

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References

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Published

07-07-2023

How to Cite

1.
Dantis K, Ramchandani R, Sahu SA, Singh VY, Dasgupta S. Primary Cutaneous Adenoid Cystic Carcinoma Of The Chest Wall With Axillary Lymph Node Metastases And Its Management: A Case Report. Rev Port Cir Cardiotorac Vasc [Internet]. 2023 Jul. 7 [cited 2024 Nov. 23];30(2):51-4. Available from: https://pjctvs.com/index.php/journal/article/view/293

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Clinical Cases

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