Endoscopic Decompression for Optic Neuropathy in McCune-Albright Syndrome

被引:1
作者
Noh, Jung-Hoon [1 ]
Kong, Doo-Sik [1 ]
Seol, Ho Jun [1 ]
Shin, Hyung Jin [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Neurosurg, Seoul 135710, South Korea
关键词
Fibrous dysplasia; McCune-Albright syndrome; Acromegaly; PITUITARY-ADENOMA; PROTEIN;
D O I
10.3340/jkns.2014.56.3.281
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
McCune-Albright syndrome (MAS) is characterized by a triad of poly/monostotic fibrous dysplasia, cafe-au-lait macules and hyperfunctioning endocrinopathies including human growth hormone excess. Acromegaly as a manifestation of endocrine hyperfunction with MAS is uncommon. Surgical excision may be challenging due to the associated severe fibrous dysplasia of the skull base. Through the endoscopic procedures, we treated a case of MAS presenting with compressive optic neuropathy due to fibrous dysplasia and acromegaly caused by growth hormone secreting pituitary adenoma. We reviewed the literature on GH excess in MAS to highlight its surgical and medical challenges.
引用
收藏
页码:281 / 283
页数:3
相关论文
共 11 条
[1]   Characterization of gsp-mediated growth hormone excess in the context of McCune-Albright syndrome [J].
Akintoye, SO ;
Chebli, C ;
Booher, S ;
Feuillan, P ;
Kushner, H ;
Leroith, D ;
Cherman, N ;
Bianco, P ;
Wientroub, S ;
Robey, PG ;
Collins, MT .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (11) :5104-5112
[2]   Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females - Report of five cases [J].
Albright, F ;
Butler, AM ;
Hampton, AO ;
Smith, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1937, 216 :727-746
[3]   MCCUNE-ALBRIGHT SYNDROME AND ACROMEGALY - CLINICAL-STUDIES AND RESPONSES TO TREATMENT IN 5 CASES [J].
CHANSON, P ;
DIB, A ;
VISOT, A ;
DEROME, PJ .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1994, 131 (03) :229-234
[4]   ATYPICAL MCCUNE-ALBRIGHT SYNDROME ASSOCIATED WITH GROWTH HORMONE-PROLACTIN PITUITARY-ADENOMA - NATURAL-HISTORY, LONG-TERM FOLLOW-UP AND SMS 201-995 - BROMOCRIPTINE COMBINED TREATMENT RESULTS [J].
CREMONINI, N ;
GRAZIANO, E ;
CHIARINI, V ;
SFORZA, A ;
ZAMPA, GA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 75 (04) :1166-1169
[5]   Transsphenoidal surgery in a patient with acromegaly and McCune-Albright syndrome: application of neuronavigation - Case report [J].
Dou, Wanchen ;
Lin, Ning ;
Ma, Wenbin ;
Yang, Yi ;
Zhu, Huijuan ;
Sun, Juan ;
Lian, Wei ;
Yang, Zhong ;
Li, Wuyi ;
Wang, Renzhi .
JOURNAL OF NEUROSURGERY, 2008, 108 (01) :164-169
[6]   GROWTH HORMONE-PROLACTIN-THYROTROPIN-SECRETING PITUITARY-ADENOMA IN ATYPICAL MCCUNE-ALBRIGHT SYNDROME WITH FUNCTIONALLY NORMAL G(S-ALPHA) PROTEIN [J].
GESSL, A ;
FREISSMUTH, M ;
CZECH, T ;
MATULA, C ;
HAINFELLNER, JA ;
BUCHFELDER, M ;
VIERHAPPER, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (04) :1128-1134
[7]   Treatment of acromegaly [J].
Holdaway, IM .
HORMONE RESEARCH, 2004, 62 :79-92
[8]   McCune-Albright syndrome: surgical and therapeutic challenges in GH-secreting pituitary adenomas [J].
Madsen, Helen ;
Borges, Manuel Thomas ;
Kerr, Janice M. ;
Lillehei, Kevin O. ;
Kleinschmidt-DeMasters, B. K. .
JOURNAL OF NEURO-ONCOLOGY, 2011, 104 (01) :215-224
[9]  
McCune DJ., 1936, Am J Dis Child, V52, P743
[10]   AN ACTIVATING G(S)ALPHA MUTATION IS PRESENT IN FIBROUS DYSPLASIA OF BONE IN THE MCCUNE-ALBRIGHT SYNDROME [J].
SHENKER, A ;
WEINSTEIN, LS ;
SWEET, DE ;
SPIEGEL, AM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (03) :750-755