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Invasive papillary breast carcinoma, solid variant with neuroendocrine differentiation
Fatma Şenel1, Hatice Karaman1, Mehtap Eroğlu1
1Clinic of Pathology, Kayseri Training and Research Hospital, Kayseri, Turkey.
Turkish Journal of Surgery
|December 21, 2017
Summary
This case report details a rare invasive papillary carcinoma, solid variant, a breast tumor found in an elderly patient. Despite its size, the tumor showed a good prognosis following surgical removal.
Area of Science:
- Oncology
- Pathology
- Radiology
Background:
- Invasive papillary carcinoma, solid variant is a rare breast malignancy.
- This tumor type typically affects elderly patients and generally has a favorable prognosis.
Purpose of the Study:
- To report a case of invasive papillary carcinoma, solid variant with neuroendocrine differentiation.
- To highlight the diagnostic and management process for this rare breast tumor.
Main Methods:
- Clinical presentation of a 72-year-old female patient with a left breast mass.
- Diagnostic workup including physical examination, mammography, and ultrasonography.
- Surgical management with modified radical mastectomy.
- Macroscopic tumor analysis.
- Histopathological and immunohistochemical analysis for definitive diagnosis.
Main Results:
- A 7 cm, well-limited, necrotic, and bleeding tumor was found in the left breast.
- The tumor occupied a significant portion of the breast area.
- Histopathological and immunohistochemical analyses confirmed invasive papillary carcinoma, solid variant with neuroendocrine differentiation.
Conclusions:
- Invasive papillary carcinoma, solid variant with neuroendocrine differentiation is a rare entity.
- Early diagnosis and surgical intervention are crucial for managing such breast tumors.
- This case contributes to the limited literature on this specific breast cancer subtype.

