Results 81 to 90 of about 9,800 (223)

Polymorphic Mucocutaneous Eruption and Septic Shock in a 75‐Year‐Old Man

JEADV Clinical Practice, Volume 5, Issue 1, Page 323-325, March 2026.
Sweta Subhadarshani, Brad R. Woodie, Kerith E. Spicknall   +2 more
wiley   +1 more source

Differences in Clinical Presentation Between Pheochromocytomas and Paragangliomas

Clinical Endocrinology, Volume 103, Issue 5, Page 651-658, November 2025.
ABSTRACT Objectives Pheochromocytomas and sympathetic paragangliomas (PPGLs) are similar in most aspects. However, they differ in genetic etiology, hormonal secretion, and associated neoplasms. This study aimed to investigate differences in clinical presentation between PPGLs. Design This study employs a retrospective cohort design. Patients The cohort
Vincent E. D. Pihlblad, Jan Calissendorff, Henrik Falhammar   +2 more
wiley   +1 more source

Syndrome of ectopic ACTH secretion in a patient without a verified tumor

Ожирение и метаболизм, 2018
Рrevalence of endogenous hypercortisilism is about 5–6 cases per 1 million people. ACTH-dependent hypercortico- sis in the general structure is about 80%.
Ekaterina V. Ershova, Evgeniya S. Senyushkina, Ekaterina A. Troshina   +2 more
doaj   +1 more source

Ectopic ACTH syndrome in a dog with a mesenteric neuroendocrine tumour: a case report [PDF]

, 2014
Ectopic ACTH secretion is provoked by extra-pituitary tumours that secrete ACTH, constituting an infrequent type of Cushing Syndrome in the dog. Neuroendocrine tumours (NET) are characterised by the synthesis of peptides with hormone activity.
Cabrera Blatter, M. F., Castillo, V. A., Galleli, M. F., García, J. D., Hall, P., Miceli, Diego Daniel, Pessina, P. P.   +6 more
core  

Effectiveness of Metyrapone in Treating Cushing's Syndrome: A Retrospective Multicenter Study in 195 Patients [PDF]

, 2015
Background: Cushing's syndrome (CS) is a severe condition with excess mortality and significant morbidity necessitating control of hypercortisolemia.
Aylwin, S., Ball, S., Boelaert, K., Cheer, K., Chortis, V., Cuthbertson, D.J., Daniel, E., Daousi, C., Davis, J., Drake, W., Grossman, A., Gunganah, K., Gurnell, M., Hill, N., Huguet, I., Karavitaki, N., Kearney, T., Lansdown, A.J., Meeran, K., Minder, A-EH., Mohit, K., Munir, A., Mustafa, O., Newell-Price, J., Powlson, A.S., Rajeev, S.P., Rees, A., Trainer, P.J.   +27 more
core   +2 more sources

Cushing’s syndrome caused by ACTH-producing thymic typical carcinoid with local invasion and regional lymph node metastasis: a case report

Surgical Case Reports, 2018
Background Ectopic ACTH-producing thymic carcinoid tumors are rare, but often behave aggressively with local invasion and distant metastasis. We herein report a case of ACTH-producing thymic typical carcinoid tumor with lymph node metastasis treated by ...
Wakako Fujiwara, Tomohiro Haruki, Yoshiteru Kidokoro, Takashi Ohno, Yohei Yurugi, Ken Miwa, Yuji Taniguchi, Hiroshige Nakamura   +7 more
doaj   +1 more source

Adrenocorticotropic hormone-producing pheochromocytoma: analysis of clinical cases

Ожирение и метаболизм, 2015
Ectopic secretion of ACTH from non-pituitary tumors, referred to as ectopic ACTH syndrome (EAS), accounts for about 10–20% of Cushing’s syndrome (CS). Ectopic hormone-secreting pheochromocytomas (Pheo) are rare.
Evgeniya Ivanovna Marova, Iya Aleksandrovna Voronkova, Anastasiya Mikhaylovna Lapshina, Svetlana Dmitrievna Arapova, Nikolay Sergeevich Kuznetsov, Lyudmila Yakovlevna Rozhinskaya, Vladimir Anatol'evich Zhivotov, Oleg Borisovich Zharkov, Larisa Evseevna Gurevich, Galina Aleksandrovna Polyakova   +9 more
doaj   +1 more source

Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women

Clinical Endocrinology, Volume 103, Issue 4, Page 540-566, October 2025.
ABSTRACT Context Androgen excess is common in women and refers to clinical or biochemical evidence of elevated androgenic steroids such as testosterone. It is associated with underlying polycystic ovary syndrome in the majority of cases. However severe androgen excess is less common and may indicate the presence of underlying adrenal or ovarian ...
Yasir S. Elhassan, James M. Hawley, Leanne Cussen, Ali Abbara, Sophie A. Clarke, Punith Kempegowda, Rima K. Dhillon‐Smith, Puja Thadani, Maureen Busby, Lucy Owusu‐Darkwah, Rachel Marrington, W. Colin Duncan, Robert K. Semple, Richard Quinton, Michael W. O'Reilly   +14 more
wiley   +1 more source

Hypokalemic metabolic alkalosis as a clinical clue to ectopic ACTH syndrome: two cases of neuroendocrine carcinoma

Endocrine Regulations
Objective. Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) is a rare, but potentially life-threatening cause of Cushing’s syndrome. Its clinical recognition may be delayed, especially when classical features of hypercortisolism are absent.
Torun Cundullah, Eken Erhan, Cakır Bahar, Uzunlulu Mehmet   +3 more
doaj   +1 more source

Ectopic adrenocorticotropic hormone syndrome associated with olfactory neuroblastoma: acquirement of adrenocorticotropic hormone expression during disease course as shown by serial immunohistochemistry examinations

Journal of International Medical Research, 2018
Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) is a condition of endogenous hypercortisolism sustained by an extrapituitary ACTH-secreting tumor.
Manabu Kadoya, Masafumi Kurajoh, Akio Miyoshi, Takuhito Shoji, Tomonori Terada, Yuji Nakamoto, Yoshitane Tsukamoto, Yuji Moriwaki, Seiichi Hirota, Hidenori Koyama   +9 more
doaj   +1 more source