Evidence map›Paper›PMID 42157024›Full record

ArticleCancer reports (Hoboken, N.J.)2026

Primary Neuroendocrine Carcinoma of the Breast: A Diagnostic Challenge and Case Report.

Hamid Zeinali Nezhad, Shima Yaghoobi, Nazanin Zeinali Nezhad, Amirhossein Shahpar, Abtin Malekpour Afshar, Mina Bagherijamebozorgi

Abstract readCase Reports
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hamid Zeinali NezhadKerman University of Medical Sciences, Kerman, Iran.ORCID 0000-0003-4331-3712
Shima YaghoobiPhysiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.ORCID 0009-0001-3948-8440
Nazanin Zeinali NezhadPhysiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.ORCID 0009-0007-9159-3487
Amirhossein ShahparGastroenterology and Hepatology Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman, Iran.ORCID 0000-0003-0003-8853
Abtin Malekpour AfsharClinical Research Development Unit, Afzalipour Hospital, Kerman University of Medical Sciences, Kerman, Iran.ORCID 0009-0006-9065-2783
Mina BagherijamebozorgiPathology and Stem Cell Research Center, Department of Pathology, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.ORCID 0009-0004-1846-4740

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary neuroendocrine carcinoma of the breast (NECB) represents an exceedingly rare entity, comprising less than 0.5% of all breast carcinomas and approximately 1% of all neuroendocrine neoplasms. The 2019 WHO classification defines NECB as tumors expressing neuroendocrine markers in > 90% of tumor cells with morphological features resembling neuroendocrine tumors of other anatomical sites. CASE PRESENTATION: A 61-year-old postmenopausal female presented with a palpable left breast mass. Clinical examination revealed a 2 × 3 cm firm, poorly circumscribed mass at the 9 o'clock position with multiple satellite lesions and a solitary axillary lymph node measuring 1.5 × 1.5 cm with rubbery consistency. Sonographic evaluation demonstrated a hypoechoic mass with spiculated margins, heterogeneous echotexture, and posterior acoustic shadowing, classified as BI-RADS 6. Core needle biopsy yielded an initial diagnosis of infiltrative ductal carcinoma, grade III, with immunohistochemistry demonstrating ER+/PR+/HER2- status and a Ki-67 index of 22%. Following modified radical mastectomy, comprehensive histopathological examination revealed distinctive neuroendocrine morphology with diffuse positivity for synaptophysin and chromogranin A, confirming the diagnosis of primary neuroendocrine carcinoma of the breast, grade 2, T2N0M0. The patient underwent multimodal therapy comprising modified radical mastectomy with sentinel lymph node biopsy (all 17 nodes negative), adjuvant anthracycline-taxane chemotherapy, chest wall radiation (50 Gy in 25 fractions), and endocrine therapy with anastrozole.

conclusionThis case highlights the diagnostic challenges of NECB, which frequently mimics conventional breast carcinoma on initial assessment. The diagnostic discordance between core biopsy and final pathology underscores the imperative for comprehensive immunohistochemical evaluation in morphologically suggestive cases. Management strategies integrate established breast cancer protocols with neuroendocrine-specific considerations, though optimal treatment paradigms remain incompletely defined due to the paucity of dedicated clinical trials for this rare entity.

Indexed as

Breast NeoplasmsCarcinoma, NeuroendocrineBiomarkers, TumorBiopsy, Large-Core NeedleBreastFemaleHumansMastectomy, Modified RadicalMiddle AgedBiomarkers, Tumorbreast carcinomadiagnostic challengesimmunohistochemistrymisdiagnosismultimodal therapyprimary neuroendocrine carcinoma

Identifiers

PMID42157024
PMCPMC13580818

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