Evidence map›Paper›PMID 41107919›Full record

ArticleDiagnostic pathology2025

Invasive breast carcinoma in a patient with PHTS: a case report.

Haiying Zhan, Neal Fischbach, Melanie Lynch, Yuanxin Liang, Uma Krishnamurti, Paul Cohen

Abstract readCase Reports
In one paragraph

Article in Diagnostic pathology, 2025. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Haiying ZhanDepartment of Pathology, Yale University School of Medicine, New Haven, CT, 06520, USA. haiying.zhan@yale.edu.
Neal FischbachDepartment of Oncology, Yale University School of Medicine, New Haven, CT, 06520, USA.
Melanie LynchDepartment of Surgery, Yale University School of Medicine, New Haven, CT, 06520, USA.
Yuanxin LiangDepartment of Pathology, Yale University School of Medicine, New Haven, CT, 06520, USA.
Uma KrishnamurtiDepartment of Pathology, Yale University School of Medicine, New Haven, CT, 06520, USA.
Paul CohenDepartment of Pathology, Yale University School of Medicine, New Haven, CT, 06520, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPTEN hamartoma tumor syndrome (PHTS) is a rare, multisystem disorder caused by germline pathogenic variants in the PTEN gene, predisposing individuals to various malignancies, including breast cancer. CASE PRESENTATION: We describe a 26-year-old woman with longstanding bilateral palpable breast masses and spontaneous bloody nipple discharge. Imaging revealed numerous cysts and masses, predominantly in the right breast. Multiple biopsies showed benign papilloma with focal atypical ductal hyperplasia (ADH), while total mastectomy specimens revealed multifocal, poorly differentiated, triple-negative invasive carcinoma. An axillary lymph node contained ectopic breast tissue with associated papillary proliferation. Genetic testing identified a pathogenic germline PTEN variant (c.209 + 4_209 + 7delAGTA), confirming PTEN hamartoma tumor syndrome (PHTS).

conclusionThis case underscores the importance of considering PHTS in young patients presenting with extensive papillomatosis and other unusual breast pathologic findings, even in the absence of a family history of cancer. Early recognition enables timely genetic counseling, confirmatory testing, and implementation of appropriate surveillance and management strategies.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastHamartoma Syndrome, MultiplePTEN PhosphohydrolaseAdultFemaleGenetic Predisposition to DiseaseGerm-Line MutationHumansPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID41107919
PMCPMC12532417

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