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Updated: Feb 8, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma

Published on: April 11, 2018

Soft Tissue Primary Neuroendocrine Tumor: A Case Report.

Nadejda Cojocari¹, Leonard David¹

¹Department of General Surgery, Fundeni Clinical Institute, Bucharest, Romania.

The American Journal of Case Reports

|July 4, 2018

Summary

This summary is machine-generated.

Primary cutaneous neuroendocrine tumors are rare, often mistaken for other conditions. This case highlights a subcutaneous abdominal neuroendocrine tumor, emphasizing the need for broader differential diagnoses in soft tissue masses.

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Establishment and Characterization of Small Bowel Neuroendocrine Tumor Spheroids

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Published on: October 14, 2019

Area of Science:

Oncology
Dermatology
Pathology

Background:

Neuroendocrine tumors (NETs) in skin/soft tissues are typically metastatic and late-stage disease indicators.
Primary cutaneous and soft tissue NETs are exceptionally rare occurrences.
Metastatic NETs often present as advanced disease manifestations.

Observation:

A case report details a 48-year-old male with a neuroendocrine tumor in subcutaneous abdominal fat.
Initial echographic appearance mimicked a vascular malformation.
Histopathological and immunohistochemical studies confirmed the neuroendocrine tumor diagnosis.

Findings:

The subcutaneous abdominal neuroendocrine tumor presented atypically on imaging.
Extensive investigations ruled out other primary internal tumor sites.
Diagnosis was confirmed through detailed histopathology and immunohistochemistry.

Implications:

Soft tissue neuroendocrine tumors can present diagnostic challenges on imaging.
These rare tumors should be considered in the differential diagnosis of soft tissue masses.
Awareness of atypical presentations is crucial for accurate diagnosis and patient management.