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A Case of Cribriform-Morular Thyroid Carcinoma Presenting Without Thyroid Nodule.
Rao, Angela; Needleman, Leor; Lalakea, M Lauren; Hsu, Emory.
Afiliação
  • Rao A; Division of Endocrinology, School of Medicine, Stanford University, Palo Alto, CA 94304, USA.
  • Needleman L; Division of Endocrinology, School of Medicine, Stanford University, Palo Alto, CA 94304, USA.
  • Lalakea ML; Department of Otolaryngology/Head and Neck Surgery, School of Medicine, Stanford University, Palo Alto, CA 94304, USA.
  • Hsu E; Santa Clara Valley Medical Center, San Jose, CA 95128, USA.
JCEM Case Rep ; 2(4): luae062, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38638335
ABSTRACT
Cribriform-morular thyroid carcinoma is a rare type of thyroid cancer. It has a strong association with familial adenomatous polyposis (FAP), a hereditary genetic disorder that predisposes individuals to the development of numerous polyps in the colon and rectum. We describe the case of a young female patient who presented with an enlarging goiter, notably without detectable thyroid nodules or masses on ultrasound, who after total thyroidectomy was found to have cribriform-morular thyroid carcinoma. This diagnosis led to genetic testing and diagnosis of FAP syndrome. We demonstrate that this rare thyroid carcinoma may present with nonsuspicious findings on sonographic evaluation while being a valuable harbinger in the diagnosis of FAP syndrome.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JCEM Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JCEM Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido