# Case Report: A rare case of cervical lymph node metastasis from prostate cancer suspicious for combined lung cancer

**Authors:** Fei-Yan Zhou, Yue Du, Fang-Hua Song, Jing-Yang Sun

PMC · DOI: 10.3389/fonc.2025.1615256 · 2025-10-13

## TL;DR

A rare case of prostate cancer metastasis to the cervical lymph node was diagnosed alongside suspected lung cancer using immunohistochemistry.

## Contribution

Demonstrates the use of IHC to distinguish prostatic origin in metastatic cancer when histopathology is limited.

## Key findings

- IHC profile confirmed prostate cancer origin in cervical lymph node metastasis.
- Case highlights the complexity of managing multiple primary cancers with atypical presentations.

## Abstract

Cervical lymph node metastasis as the initial manifestation of prostate cancer is uncommon, and the diagnostic and therapeutic processes become considerably more complex when primary lung malignancy is also suspected. Immunohistochemical (IHC) techniques are critical in the diagnosis of multiple primary malignancies, in particular when histopathologic access is limited. We report on a 74-year-old male patient who presented with respiratory symptoms. Computed tomography revealed a 6.4-cm × 4.7-cm mass in the upper lobe of the right lung with cervical lymph node metastasis. The initial diagnosis of metastatic adenocarcinoma was established by cervical lymph node biopsy. During follow-up, the patient developed progressive dysuria, and prostate cancer was ultimately confirmed by prostate biopsy. IHC analysis of the cervical lymph node specimen revealed the following profile: prostate-specific antigen (PSA) (focally positive, 3+), P504S (diffusely positive, 3+), TTF1 (−), CK7 (−), CK20 (−), napsin A (−), and P40 (−). This IHC profile definitively established the prostatic origin of the metastatic carcinoma in the cervical lymph node. This case highlights the value of employing therapeutic diagnostic strategies when definitive histopathologic access is challenging and provides insights into the management of atypical metastatic prostate cancer and multiple primary cancers.

## Linked entities

- **Proteins:** KLK3 (kallikrein related peptidase 3), AMACR (alpha-methylacyl-CoA racemase), TTF1 (transcription termination factor 1), KRT7 (keratin 7), KRT20 (keratin 20), Napsa (napsin A aspartic peptidase), IL9 (interleukin 9)
- **Diseases:** prostate cancer (MONDO:0005159), lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** TTF1 (transcription termination factor 1) [NCBI Gene 7270] {aka TTF-1, TTF-I}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, NAPSA (napsin A aspartic peptidase) [NCBI Gene 9476] {aka KAP, Kdap, NAP1, NAPA, NR1H2-AS1, SNAPA}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** lung cancer (MESH:D008175), adenocarcinoma (MESH:D000230), dysuria (MESH:D053159), prostate cancer (MESH:D011471), Cervical lymph node metastasis (MESH:D008207), cancers (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** P504S

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12554590/full.md

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Source: https://tomesphere.com/paper/PMC12554590