Pregled bibliografske jedinice broj: 1070536
Vandetanib in medullary thyroid cancer-related Cushing syndrome: a case report
Vandetanib in medullary thyroid cancer-related Cushing syndrome: a case report // Endocrine Abstracts 67
Atena: BioScientifica, 2019. str. 28-28 doi:10.1530/endoabs.67.GP5 (poster, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 1070536 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Vandetanib in medullary thyroid cancer-related Cushing
syndrome: a case report
Autori
Režić, Tanja ; Matijaca, Ana ; Škorić Polovina, Tanja ; Marušić, Srećko ; Pandžić Jakšić, Vlatka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Endocrine Abstracts 67
/ - Atena : BioScientifica, 2019, 28-28
Skup
7th ESE Young Endocrinologists and Scientists (EYES) Meeting
Mjesto i datum
Atena, Grčka, 13.09.2019. - 15.09.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
vandetanib, medullary thyroid cancer, Cushing syndrome
(vandetanib, medullary thyroid cancer, Cushing syndrom)
Sažetak
Background: Medullary thyroid cancer is a rare neuroendocrine neoplasm that can secrete variety of hormones, including ACTH. Cushing syndrome due to ectopic ACTH secretion is a rare complication of medullary thyroid cancer, usually accociated with metastatic disease. Around 50 percent of patients with medullary thyroid carcinoma and ectopic Cushing syndrome die due to complications of hypercortisolism. Based on the aforementioned, efficient management of hypercortisolism is crucial. Case presentation: A 44-year old female with history of metastatic medullary thyroid cancer presented with malaise, generalized oedema, hypertension, hirsutism, fragile skin and finger ulceration. Laboratory results showed marked hypokaliemia and hyperglicaemia. The diagnosis of Cushing syndrome due to ectopic ACTH secretion was made. The patient was initially treated with ketoconazole, followed by metyrapone and vandetanib. After introduction of metyrapone and vandetanib, a rapid decrease in serum cortisol and improvement of clinical symptoms were observed as well as the reduction of tumor metastases. As an adverse effect to vandetanib, the patient developed palmar-plantar erythrodysestesia. The rash resolved after topical cotrticosteroid treatment. Conclusion: Management of Cushing syndrome in medullary thyroid carcinoma is challenging. Use of drugs, such as steroid inhibitors, is often unsuccessful and bilateral adrenalectomy is sometimes required. In recent years, the use of tyrosine kinase inhibitors, especially vandetanib, has been shown to successfully control hypercortisolism. Despite adverse effects, some of which are potenially serious, vandetanib is an important and efficient drug in the achievment of eucortisolism in patients with medullary thyroid cancer-related Cushing syndrome as well as in inducing tumor control.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinička bolnica "Dubrava"