Pituitary Blastoma in a 19-Year-Old Woman: A Case Report and Review of Literature

被引:8
作者
Chhuon, Youliny [1 ]
Weon, Young Cheol [1 ]
Park, Gyeongmin [1 ]
Kim, Misung [2 ]
Park, Jun Bum [3 ]
Park, Sang Kyu [4 ]
机构
[1] Univ Ulsan, Coll Med, Dept Radiol, Ulsan Univ Hosp, Ulsan, South Korea
[2] Univ Ulsan, Coll Med, Dept Pathol, Ulsan Univ Hosp, Ulsan, South Korea
[3] Univ Ulsan, Coll Med, Dept Neurosurg, Ulsan Univ Hosp, Ulsan, South Korea
[4] Univ Ulsan, Coll Med, Dept Pediat, Ulsan Univ Hosp, Ulsan, South Korea
关键词
Adult; Case report; Magnetic resonance imaging; Pathology; Pituitary blastoma; TUMORS; GLAND;
D O I
10.1016/j.wneu.2020.04.096
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Pituitary blastoma is a malignant neoplasm of the pituitary gland that was recognized by the World Health Organization in 2017. It is commonly diagnosed in children before 24 months of age. Here, we report the first case of a young adult patient who was diagnosed with pituitary blastoma with increased levels of growth hormone instead of adrenocorticotropic hormone and provide a review of the literature. CASE DESCRIPTION: A 19-year-old woman presented to our hospital with visual disturbance. She had a medical history of Wilms' tumor and multinodular goiter. The brain imaging showed a 3.2 x 2.5 x 1.8-cm solid sellar and suprasellar cystic mass that upwardly displaced the optic chiasm. She had an elevated level of growth hormone but a normal level of adrenocorticotropic hormone, cortisol, and prolactin. The mass was subtotally removed through the left pterional craniotomy. The pathologic examination suggested a pituitary blastoma. Thereafter, the patient was treated with chemotherapy and radiotherapy. At 4-year follow-up postsurgery, her overall well-being is good. CONCLUSIONS: Although in this case the patient was a young adult, pituitary blastoma should be taken into consideration when children have an enhanced sellar and suprasellar mass with peripherally located cysts.
引用
收藏
页码:310 / 313
页数:4
相关论文
共 16 条
[11]   Germline and Somatic DICER1 Mutations in a Pituitary Blastoma Causing Infantile-Onset Cushing's Disease [J].
Sahakitrungruang, Taninee ;
Srichomthong, Chalurmpon ;
Pornkunwilai, Sopon ;
Amornfa, Jiraporn ;
Shuangshoti, Shanop ;
Kulawonganunchai, Supasak ;
Suphapeetiporn, Kanya ;
Shotelersuk, Vorasuk .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2014, 99 (08) :E1487-E1492
[12]   Pituitary blastoma [J].
Scheithauer, Bernd W. ;
Kovacs, Kalman ;
Horvath, Eva ;
Kim, D. S. ;
Osamura, Robert Y. ;
Ketterling, Rhett P. ;
Lloyd, Ricardo V. ;
Kim, O. L. .
ACTA NEUROPATHOLOGICA, 2008, 116 (06) :657-666
[13]   Pituitary blastoma: a unique embryonal tumor [J].
Scheithauer, Bernd W. ;
Horvath, E. ;
Abel, T. W. ;
Robital, Y. ;
Park, S. -H. ;
Osamura, R. Y. ;
Deal, C. ;
Lloyd, R. V. ;
Kovacs, K. .
PITUITARY, 2012, 15 (03) :365-373
[14]   DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies [J].
Schultz, Kris Ann P. ;
Williams, Gretchen M. ;
Kamihara, Junne ;
Stewart, Douglas R. ;
Harris, Anne K. ;
Bauer, Andrew J. ;
Turner, Joyce ;
Shah, Rachana ;
Schneider, Katherine ;
Schneider, Kami Wolfe ;
Carr, Ann Garrity ;
Harney, Laura A. ;
Baldinger, Shari ;
Frazier, A. Lindsay ;
Orbach, Daniel ;
Schneider, Dominik T. ;
Malkin, David ;
Dehner, Louis P. ;
Messinger, Yoav H. ;
Hill, D. Ashley .
CLINICAL CANCER RESEARCH, 2018, 24 (10) :2251-2261
[15]   Endoscopic Transsphenoidal Approach for Resection of Malignant Pituitary Blastoma in an 18-Month-Old Infant: A Technical Note [J].
Zaben, Malik ;
Zafar, Mohsin ;
Bukhari, Shafqat ;
Leach, Paul ;
Hayhurst, Charoline .
OPERATIVE NEUROSURGERY, 2014, 10 (04) :649-653
[16]  
Zada G, 2016, ATLAS SELLAR PARASEL, P197