A Case of Small Cell Cancer of the Breast in a Male with Synchronous Stage IV Non-Small Cell Lung Carcinoma

Matt, Laurie; Limjoco, Teresa; Sehgal, Rajesh

doi:10.4081/rt.2013.e52

Cited by 1 publication

(1 citation statement)

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“…We note that, while patients were mostly females, 4 cases were reported in males (a higher proportion than would typically be expected in breast cancer). [17,36,44,58] Interestingly, more patients were found to be non-smokers, in contrast to what would be commonly seen in lung SCC. [3,4,8,14,27,38,43,68] There are no unique imaging characteristics that help differentiate SCC from invasive ductal carcinomas in the breast.…”

Section: Discussion and Literature Reviewmentioning

confidence: 95%

Evolution of an invasive ductal carcinoma to a small cell carcinoma of the breast

et al. 2022

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Rationale: Small cell carcinoma (SCC) is a rare subtype of breast cancer and presents a complex diagnostic and treatment challenge, due to paucity of data. To the best of our knowledge, most cases of breast SCC reported in the literature describe a de novo breast primary. Our case is unique as it describes the evolution of an invasive ductal carcinoma after treatment into a SCC of the breast. Patient concerns and diagnosis: We report a case of a 53-year-old female, lifelong non-smoker, who initially presented with breast mass noted on self examination. Breast and axillary lymph node biopsy demonstrated a hormone receptor positive invasive ductal carcinoma with a metastatic T3 lesion. Intervention: She was treated with first-line palbociclib/letrozole with initial clinical response, and at progression was switched to capecitabine with no response. Repeat biopsy of the axillary lesion showed evolution of the tumor into a triple negative breast cancer. She was then treated with third-line paclitaxel and radiation therapy with good initial response. She eventually had further disease progression and presented with a new mediastinal lymphadenopathy causing SVC syndrome. Biopsy of this showed a small cell variant of breast neuroendocrine carcinoma. Due to the evolution of histology in this case, a retrospective review of her initial breast specimen as well as the second biopsy from the axilla was conducted which confirmed that the mediastinal lymphadenopathy was metastatic from the original breast tumor. Outcomes and lessons: We speculate that the initial treatment allowed a minority of treatment-resistant neuroendocrine cells to grow and become the dominant face of the tumor. Our patient had an excellent response to carboplatin/etoposide and consolidative locoregional radiotherapy but presented with an early intracranial recurrence. This is a similar pattern of metastases as seen in lung SCC and highlights a potential role for prophylactic cranial irradiation in breast SCC. Further studies are needed to better understand the biology and treatment of breast SCC which continues to present a challenge for clinicians.

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