Scopus
🔓 Açık Erişim YÖKSİS DOI Eşleşti
SJR Q4
A rare combination: Multiple endocrine neoplasia type 1 and follicular thyroid carcinoma
Turkish Journal of Endocrinology and Metabolism · Ocak 2020
YÖKSİS Kayıtları
A Rare Combination: Multiple Endocrine Neoplasia Type 1 and Follicular Thyroid Carcinoma
TURKISH JOURNAL OF ENDOCRINOLOGY AND METABOLISM · 2020 Web of Science
Dr. Öğr. Üyesi AHMET GÖRGEL →
YÖKSİS Kayıtları — ISSN Eşleşmesi
The Frequency of Thyroid Diseases in Women with Breast Cancer
2018 ISSN: 1301-2193 ESCI
Prof. Dr. HANDE KÖKSAL →
Serum Endocan Level and Its Correlation with Clinicopathologic Features in Patients with Papillary Thyroid Cancer
2022 ISSN: 1301-2193 ESCI
Prof. Dr. FATMA HÜMEYRA YERLİKAYA AYDEMİR →
Serum Endocan Level and Its Correlation with Clinicopathologic Features in Patients with Papillary Thyroid Cancer
2022 ISSN: 1301-2193 ESCI
Prof. Dr. FATMA HÜMEYRA YERLİKAYA AYDEMİR →
Serum Endocan Level and Its Correlation with Clinicopathologic Features in Patients with Papillary Thyroid Cancer
2022 ISSN: 1301-2193 Scopus
Prof. Dr. FATMA HÜMEYRA YERLİKAYA AYDEMİR →
Does Glucagon-Like Peptide-1 Have a Role in the Etiopathogenesis of Gestational Diabetes?
2016 ISSN: 1301-2193 Web of Science
Dr. Öğr. Üyesi AHMET GÖRGEL →
A Rare Combination: Multiple Endocrine Neoplasia Type 1 and Follicular Thyroid Carcinoma
2020 ISSN: 1301-2193 Web of Science
Dr. Öğr. Üyesi AHMET GÖRGEL →
Serum Endocan Level and Its Correlation with Clinicopathologic Features in Patients with Papillary Thyroid Cancer
2022 ISSN: 1301-2193 TR DİZİN
Öğr. Gör. MUSA KÜRŞAD ŞENER →
Makale Bilgileri
ISSN13012193
Yayın TarihiOcak 2020
Cilt / Sayfa24 · 87-91
Scopus ID2-s2.0-85081557241
Erişim🔓 Açık Erişim
Özet
Multiple endocrine neoplasia Type 1 (MEN-1) is an inherited syndrome characterized by the development of endocrine tumors of the pancreas, parathyroid, and pituitary glands. Mesenchymal tumors and adrenal neoplasms might also accompany this syndrome. However, the syndrome is rarely associated with thyroid tumors in contrary to the multiple endocrine neoplasia Type 2 that includes medullary thyroid carcinoma. This case study presents a 44-year-old woman who was diagnosed with MEN-1 on the basis of her clinical characteristics, laboratory data, and the presence of endocrine tumors. Follicular thyroid carcinoma was detected in the patient when she was being operated for nodular goiter, 12 years ago. We report this rare case which is likely the third case in the available scientific literature.
Yazarlar (4)
1
Ahmet Gorgel
2
Sacit Nuri Görgel
3
Mustafa Demirpençe
4
Mitat Bahçeci
Anahtar Kelimeler
Acromegaly
Follicular thyroid carcinoma
Hypoglycemia
Multiple endocrine neoplasia Type 1
Nephrolithiasis
Kurumlar
Ataturk Training and Research Hospital
Izmir Turkey
Scimago Dergi (ISSN Eşleşmesi)
Turkish Journal of Endocrinology and Metabolism
Q4
OA
SJR Skoru0,121
YayıncıAVES Ibrahim KARA
ÜlkeTurkey
Endocrinology, Diabetes and Metabolism (Q4)
Internal Medicine (Q4)