Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome
Patients with Beckwith-Wiedemann syndrome (BWS) are predisposed to developing embryonal tumors, with hepatoblastoma being the most common type. Our patient showed hemihypertrophy, macroglossia, and paternal uniparental disomy in chromosome 11 and was diagnosed with BWS. When the patient was 9 months...
Saved in:
Main Authors: | Eun Na Kim (Author), Dong Eun Song (Author), Hee Mang Yoon (Author), Beom Hee Lee (Author), Chong Jai Kim (Author) |
---|---|
Format: | Book |
Published: |
Korean Society of Pathologists & the Korean Society for Cytopathology,
2019-03-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Adrenal masses associated with Beckwith Wiedemann syndrome in the newborn
by: Taide Devendra, et al.
Published: (2010) -
Diagnosis and Management of Beckwith-Wiedemann Syndrome
by: Kathleen H. Wang, et al.
Published: (2020) -
An Intrarenal Adrenocortical Carcinoma Arising in an Adrenal Rest
by: Ji Hee Lee, et al.
Published: (2018) -
A Case of BeckwithWiedemann Syndrome with Polyhydramnios
by: Yusrawati Yusrawati, et al.
Published: (2017) -
ADRENAL CORTICAL CARCINOMA IN INFANCY
by: Carlos Alberto Longui