# Synchronous double primary small cell lung cancer and invasive ductal breast carcinoma: a case report

**Authors:** Junqing Gan, Meiyue Liu, Fei Liu, Junxiu Wen, Wenjuan Fu, Jinghao Jia

PMC · DOI: 10.1186/s12890-024-02897-y · BMC Pulmonary Medicine · 2024-02-22

## TL;DR

A 75-year-old woman was diagnosed with two rare cancers at the same time: small cell lung cancer and invasive breast cancer, making this a unique medical case.

## Contribution

This is the first reported case of synchronous primary small cell lung cancer and invasive ductal breast carcinoma.

## Key findings

- The patient had a 4.2 cm lung mass confirmed as small cell lung cancer and a 3.8 cm breast lesion diagnosed as invasive ductal carcinoma.
- Immunohistochemistry confirmed distinct markers for both cancers, supporting their independent origins.
- Brain metastases were detected, leading to a treatment plan involving radiation and chemotherapy.

## Abstract

Although lung and breast cancers are common malignancies, the occurrence of primary synchronous neoplasms involving these organs has been rarely reported in literature.

A 75-year-old female patient presented at a local hospital with a ten-day history of dizziness and slurred speech. A CT contrast-enhanced scan revealed a 4.2 cm mass in the lower lobe of the right lung and a 3.8 cm space-occupying lesion in the right breast. Subsequent breast ultrasound identified a hypoechoic lesion measuring5.41 × 4.75 × 3.06 cm in the right breast, and an ultrasound-guided biopsy confirmed the presence of infiltrating ductal carcinoma of the right breast. The immunohistochemistry analysis of the breast mass revealed positive staining for ER, PR, HER-2, AR and Ki67 in the tumor cells, while negative staining was observed for P63, Calponin, CK5/6 and CK14. MR imaging of the head detected abnormal signals in the right frontal lobe (3.6 cm×2.9 cm in size), left cerebellar hemisphere, and punctate enhancement in the left temporal lobe, indicating potential metastasis. Pathological examination of a lung biopsy specimen confirmed the presence of small cell lung cancer (SCLC). Furthermore, immunohistochemistry analysis of the lung lesions demonstrated positive staining for TTF-1, CK-Pan, Syn, CgA, CD56, P53 (90%) and Ki67 (70%), and negative staining for NapsinA and P40 in the tumor cells. The patient’s diagnosis of SCLC with stage cT2bN0M1c IVB and brain metastases (BM), as well as invasive ductal breast carcinoma (IDC), was confirmed based on the aforementioned results. Whereupon we proposed a treatment plan consisting of whole-brain radiation (40 Gy/20fractions), focal radiotherapy (60 Gy/20fractions), and adjuvant concurrent chemotherapy with oral etoposide (50 mg on days 1 to 20).

To the best of our knowledge, the present case is the first of its kind to describe the synchronous double cancer, consisting of primary SCLC and IDC.

## Linked entities

- **Proteins:** EREG (epiregulin), PGR (progesterone receptor), ERBB2 (erb-b2 receptor tyrosine kinase 2), AR (androgen receptor), Mki67 (antigen identified by monoclonal antibody Ki 67), RPE65 (retinoid isomerohydrolase RPE65), Chd64 (transgelin calponin-3), ck56 (hypothetical protein), KRT14 (keratin 14), TTF1 (transcription termination factor 1), FYN (FYN proto-oncogene, Src family tyrosine kinase), CGA (glycoprotein hormones, alpha polypeptide), NCAM1 (neural cell adhesion molecule 1), TP53 (tumor protein p53), Napsa (napsin A aspartic peptidase), IL9 (interleukin 9)
- **Chemicals:** etoposide (PubChem CID 36462)
- **Diseases:** small cell lung cancer (MONDO:0008433), invasive ductal breast carcinoma (MONDO:0004953)

## Full-text entities

- **Genes:** NAPSA (napsin A aspartic peptidase) [NCBI Gene 9476] {aka KAP, Kdap, NAP1, NAPA, NR1H2-AS1, SNAPA}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, NCAM1 (neural cell adhesion molecule 1) [NCBI Gene 4684] {aka CD56, MSK39, NCAM}, KRT14 (keratin 14) [NCBI Gene 3861] {aka CK14, EBS1, EBS1A, EBS1B, EBS1C, EBS1D}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, TTF1 (transcription termination factor 1) [NCBI Gene 7270] {aka TTF-1, TTF-I}, SYNM (synemin) [NCBI Gene 23336] {aka DMN, SYN}, CHGA (chromogranin A) [NCBI Gene 1113] {aka CGA, PHE5, PHES}
- **Diseases:** breast mass (MESH:D061325), IDC (MESH:D018270), lung and breast cancers (MESH:D001943), double cancer (MESH:D009369), dizziness (MESH:D004244), SCLC (MESH:D055752), metastasis (MESH:D009362), infiltrating ductal carcinoma of (MESH:D044584), lung lesions (MESH:D008171), BM (MESH:D001932)
- **Chemicals:** etoposide (MESH:D005047)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC10885399/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10885399/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC10885399/full.md

---
Source: https://tomesphere.com/paper/PMC10885399