AI Article Synopsis
- Neuroendocrine synchronous multiplicity carcinoma is rare, typically requiring both imaging and pathological confirmation for diagnosis, with few cases combining pathology and immunohistochemistry.
- A patient presenting with abdominal pain was found to have tumors in both the small intestine and lung, diagnosed as neuroendocrine carcinomas through imaging and pathology.
- The treatment involved surgical resection of the intestinal lesion and chemoradiotherapy for the lung tumor, resulting in a survival time exceeding 24 months, highlighting the importance of comprehensive diagnostic methods in managing this condition.
Article Abstract
Rationale: In clinical work, neuroendocrine synchronous multiplicity carcinoma was relatively rare. Most were confirmed by the pathological diagnosis of a certain part of the body combined with the imaging of the whole body, while cases that had both pathological and immunohistochemistry diagnosis were few.
Patient Concerns: A patient who presented with abdominal pain visited our hospital, and was diagnosed with lesions in both the small intestine and lung.
Diagnoses: Both were considered primary tumors by imaging, and diagnosed as neuroendocrine carcinomas by pathology.
Interventions: The intestinal lesion was surgically resected, and the lung tumor treated by chemoradiotherapy.
Outcomes: The survival time of this patient exceeded 24 months.
Lessons: The diagnosis relied on clinical, imaging, pathological, and immunohistochemical features, which confirmed a synchronous multiple carcinoma. Treatment was based on the pathological types. Through this case report, the clinical and pathological data of neuroendocrine synchronous multiplicity carcinoma could be enriched.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5690789 | PMC |
| http://dx.doi.org/10.1097/MD.0000000000008623 | DOI Listing |
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