Abstract

BackgroundThe incidence of superior vena cava syndrome within the United States is roughly 15,000 cases per year. Superior vena cava syndrome is a potentially life-threatening medical condition; however, superior vena cava syndrome is not fatal in the majority of cases. Superior vena cava syndrome encompasses a collection of signs and symptoms resulting from obstruction of the superior vena cava, including swelling of the upper body of the head, neck, arms, and/or breast. It is also associated with cyanosis, plethora, and distended subcutaneous vessels. Lung cancer, including both non-small cell lung cancer and small cell lung cancer, is the most common extrinsic cause of superior vena cava syndrome. Intrinsic disruption of superior vena cava flow can also precipitate superior vena cava syndrome. This case report describes an unusual presentation and potential etiology of superior vena cava syndrome.Case presentationOur patient was a 51-year-old black woman with locally advanced, stage IIIB non-small cell lung cancer who had no clinical symptoms of superior vena cava syndrome at the time of diagnosis. However, she did have radiographic evidence of superior vena cava stenosis caused by extrinsic compression from her large right hilar primary tumor. She was treated with definitive chemoradiation, receiving 60 Gy of external beam radiation therapy given concurrently with chemotherapy. Three months after completion of radiotherapy, she developed signs of superior vena cava syndrome, including breast and supraclavicular swelling. She had a chest computed tomography scan showing over 50% reduction in the size of a right hilar mass; however, she had continued radiographic stenosis of the superior vena cava. The distribution of stenosis appeared to be inferior to the caudal extent of pretreatment tumor volume. She had no other radiographic indications for superior vena cava syndrome.ConclusionsGenerally, superior vena cava syndrome is the result of extrinsic compression of the superior vena cava by tumor. Our patient’s case represents the development of superior vena cava syndrome after an excellent response of tumor with near-complete tumor response. We suspect chemoradiation therapy as a potential etiology for the precipitation of the superior vena cava syndrome, which is currently not well reported in the medical literature.

Highlights

  • The incidence of superior vena cava syndrome within the United States is roughly 15,000 cases per year

  • Radiation is suspected as the direct cause of Superior vena cava (SVC) syndrome in our patient, which adds to the paucity of data portraying radiation as an etiology of SVC syndrome

  • It is possible that the development of the SVC syndrome was a chemoradiation-related event, but it is not uncommon for the SVC to get the full dose of radiation in the treatment of thoracic malignancies

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Summary

Conclusions

Our patient’s case differs from the previously mentioned cases in that the formation of the SVC syndrome occurred just 3 months after the completion of radiotherapy, much earlier than previously reported. The unique part of our patient’s case is the fact that development of SVC syndrome coincided with remarkable reduction in the size of her tumor and presumed lessening of the extrinsic compression. It is possible that the development of the SVC syndrome was a chemoradiation-related event, but it is not uncommon for the SVC to get the full dose of radiation in the treatment of thoracic malignancies. It was considered that the SVC syndrome could be related to microscopic extension of the tumor beyond what could be identified on imaging studies. All authors read and approved the final manuscript. Ethics approval and consent to participate Written informed consent was obtained from the patient for publication of this case report and any accompanying images. 720 Eskenazi Avenue, Fifth Third Bank Building 3rd Floor, Indianapolis, IN 46202, USA. 4Department of Hematology and Oncology, Indiana University School of Medicine, 980 West Walnut Street R3 C312, Indianapolis, IN 46202, USA

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