# Silent Yet Striking: Medullary Carcinoma Behind an Intestinal Obstruction

**Authors:** Nasim Salimiaghdam, Ahmed Mustafa, Irene O Pokuaa, Afshin Hamidi, Emily Chen

PMC · DOI: 10.7759/cureus.86669 · Cureus · 2025-06-24

## TL;DR

A rare case of medullary carcinoma in the ascending colon is reported, highlighting its unique features and management.

## Contribution

This case report provides insights into the clinical presentation and management of a rare medullary subtype of colorectal cancer.

## Key findings

- The tumor was pT3N0M0, G3 stage II with microsatellite instability (MSI-H) due to loss of MLH1 and PMS2.
- Adjuvant chemotherapy was not required due to absence of nodal involvement.
- Follow-up included CEA monitoring, imaging, and colonoscopy despite CEA's low sensitivity in medullary cancer.

## Abstract

Carcinoma of the ascending colon, especially the medullary type, is a rare and poorly differentiated form of colorectal cancer. This case report details a case of a 75-year-old woman with a background of cardiovascular issues, hypertension, and dementia who presented with complete large bowel obstruction and was found to have poorly differentiated carcinoma of the ascending colon with medullary features. The surgical approach involved an exploratory laparotomy followed by a right hemicolectomy. The pathological analysis confirmed a pT3N0M0, G3 stage II tumor, characterized by a loss of MLH1 and PMS2 protein expression, indicating microsatellite instability (MSI-H). Since there was no nodal involvement, adjuvant chemotherapy wasn’t deemed necessary. The patient was encouraged to keep up with regular follow-ups, which would include monitoring carcinoembryonic antigen (CEA) levels, a complete metabolic panel (CMP), a complete blood count (CBC), and CT imaging every six months and annually. Although CEA is the most established tumor marker in colorectal cancer, it is still part of the follow-up plan, owing to its lack of sensitivity in the medullary subtype. In addition to this, the recommendation was for a surveillance colonoscopy every three years.

This report sheds light on the case’s pathological, clinical, and follow-up elements, emphasizing the need for personalized patient management.

## Linked entities

- **Proteins:** MLH1 (mutL homolog 1), PMS2 (PMS1 homolog 2, mismatch repair system component)
- **Diseases:** dementia (MONDO:0001627), colorectal cancer (MONDO:0005575), medullary carcinoma (MONDO:0015277)

## Full-text entities

- **Genes:** PMS2 (PMS1 homolog 2, mismatch repair system component) [NCBI Gene 5395] {aka HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMSL2}, MLH1 (mutL homolog 1) [NCBI Gene 4292] {aka COCA2, FCC2, HNPCC, HNPCC2, LYNCH2, MLH-1}
- **Diseases:** colorectal cancer (MESH:D015179), large bowel obstruction (MESH:D012778), stage II tumor (MESH:D009369), nodal (MESH:D013611), dementia (MESH:D003704), hypertension (MESH:D006973), microsatellite instability (MESH:D053842), MSI-H (MESH:D000848), Carcinoma of the ascending colon (MESH:D003110), Medullary Carcinoma (MESH:D018276)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12288939/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12288939/full.md

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Source: https://tomesphere.com/paper/PMC12288939