التفاصيل البيبلوغرافية
| العنوان: |
Beckwith–Wiedemann syndrome with juvenile fibrous nodules and lobular breast tumors: a case report and review of the literature. |
| المؤلفون: |
Sato, Yo, Watanabe, Yusuke, Morisaki, Takafumi, Hayashi, Saori, Otsubo, Yoshiki, Ochiai, Yurina, Mizoguchi, Kimihisa, Takao, Yuka, Yamada, Mai, Mizuuchi, Yusuke, Nakamura, Masafumi, Kubo, Makoto |
| المصدر: |
Surgical Case Reports; 3/22/2024, Vol. 10 Issue 1, p1-7, 7p |
| مصطلحات موضوعية: |
LOBULAR carcinoma, LITERATURE reviews, BREAST tumors, GENOMIC imprinting, CORE needle biopsy, UMBILICAL hernia |
| مستخلص: |
Background: Beckwith–Wiedemann syndrome (BWS) is a genomic imprinting disorder caused by diverse genetic and/or epigenetic disorders of chromosome 11p15.5. BWS presents with a variety of clinical features, including overgrowth and an increased risk of embryonal tumors. Notably however, reports of patients with BWS and breast tumors are rare, and the association between these conditions is still unclear. Insulin-like growth factor-2 (IGF2) expression is known to be associated with the development of various cancers, including breast cancer, and patients with BWS with specific subtypes of molecular defects are known to show characteristic clinical features and IGF2 overexpression. Case presentation: A 17-year-old girl who had been diagnosed with BWS based on an umbilical hernia, hyperinsulinemia, and left hemihypertrophy at birth, visited our department with a gradually swelling left breast. Her left breast was markedly larger than her right breast on visual examination. Imaging examinations showed two tumors measuring about 10 cm each in the left breast, and she was diagnosed with juvenile fibroadenoma following core needle biopsy. The two breast tumors were removed surgically and the patient remained alive with no recurrence. The final diagnosis was juvenile fibroadenoma without malignant findings. Immunohistochemical staining using IGF2 antibody revealed overexpression of IGF2 in the cytoplasm of ductal epithelial cells. Because of her clinical features and IGF2 overexpression, molecular defects of 11p15.5 including a possible genetic background of paternal uniparental disomy of chromosome 11 or hypermethylation of imprinting center 1 was suspected. Conclusions: In this case, overexpression of IGF2 suggested a possible relationship between BWS and breast tumors. Moreover, the characteristic clinical features and IGF2 staining predicted the subtype of 11p15.5 molecular defects in this patient. [ABSTRACT FROM AUTHOR] |
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