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Gokalp, D., Tuzcu, A., Bahceci, M., Arikan, S., Bahceci, S. and Pasa, S. (2009) Sheehan’a syndrome as a rare cause of anaemia secondary to hypopituitarism. Annals of Hematology, 88, 405-410.
http://dx.doi.org/10.1007/s00277-008-0607-4

has been cited by the following article:

• TITLE: A decade without diagnosis: Sheehan’s syndrome

  AUTHORS: Fábio A. Nascimento, Juliane Nery, Gustavo Lenci Marques, Felipe Dunin dos Santos, Mauricio de Carvalho

  KEYWORDS: Sheehan’s Syndrome; Pituitary Insufficiency; Empty Sella

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.2 No.8, November 14, 2013

  ABSTRACT: Sheehan’s Syndrome (SS) occurs as a result of ischemic pituitary necrosis due to severe post-partum hemorrhage. We report a 41-year-old woman with a history of severe postpartum hemorrhage 18 years prior to presentation. During this period of time, she experienced severe fatigue. Three months prior to being admitted to our hospital, the patient started to notice alopecia, generalized edema and cognitive impairment. After proper investigation, laboratory tests and clinical findings indicated panhypopituitarism. In addition to neuroimaging and past medical history, SS was diagnosed and treatment started. We emphasize the importance of thorough investigation, further diagnosis and management of this condition (especially in third world countries), since SS is a neurological and endocrinological emergency and potentially life threatening.