A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up

Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was refer...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Honda, Tomoko [verfasserIn] Itoh, Fumiko [verfasserIn] Nakamura, Kimitoshi [verfasserIn] Ohba, Takashi [verfasserIn] Katabuchi, Hidetaka [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2016

Schlagwörter:	Fibrous dysplasia of bone McCune–Albright syndrome Positron-emission tomography Precocious pseudopuberty Sexual precocity

Übergeordnetes Werk:	Enthalten in: Reproductive medicine and biology - Hoboken, NJ : Wiley, 2002, 15(2016), 4 vom: 15. Apr., Seite 261-265
Übergeordnetes Werk:	volume:15 ; year:2016 ; number:4 ; day:15 ; month:04 ; pages:261-265

Links:	Volltext

DOI / URN:	10.1007/s12522-016-0242-z

Katalog-ID:	SPR026013460

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520			\|a Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary.
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allfields	10.1007/s12522-016-0242-z doi (DE-627)SPR026013460 (SPR)s12522-016-0242-z-e DE-627 ger DE-627 rakwb eng 610 ASE 42.23 bkl 44.74 bkl 44.92 bkl Honda, Tomoko verfasserin aut A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary. Fibrous dysplasia of bone (dpeaa)DE-He213 McCune–Albright syndrome (dpeaa)DE-He213 Positron-emission tomography (dpeaa)DE-He213 Precocious pseudopuberty (dpeaa)DE-He213 Sexual precocity (dpeaa)DE-He213 Itoh, Fumiko verfasserin aut Nakamura, Kimitoshi verfasserin aut Ohba, Takashi verfasserin aut Katabuchi, Hidetaka verfasserin aut Enthalten in Reproductive medicine and biology Hoboken, NJ : Wiley, 2002 15(2016), 4 vom: 15. Apr., Seite 261-265 (DE-627)349876223 (DE-600)2081579-7 1447-0578 nnns volume:15 year:2016 number:4 day:15 month:04 pages:261-265 https://dx.doi.org/10.1007/s12522-016-0242-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 42.23 ASE 44.74 ASE 44.92 ASE AR 15 2016 4 15 04 261-265
spelling	10.1007/s12522-016-0242-z doi (DE-627)SPR026013460 (SPR)s12522-016-0242-z-e DE-627 ger DE-627 rakwb eng 610 ASE 42.23 bkl 44.74 bkl 44.92 bkl Honda, Tomoko verfasserin aut A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary. Fibrous dysplasia of bone (dpeaa)DE-He213 McCune–Albright syndrome (dpeaa)DE-He213 Positron-emission tomography (dpeaa)DE-He213 Precocious pseudopuberty (dpeaa)DE-He213 Sexual precocity (dpeaa)DE-He213 Itoh, Fumiko verfasserin aut Nakamura, Kimitoshi verfasserin aut Ohba, Takashi verfasserin aut Katabuchi, Hidetaka verfasserin aut Enthalten in Reproductive medicine and biology Hoboken, NJ : Wiley, 2002 15(2016), 4 vom: 15. Apr., Seite 261-265 (DE-627)349876223 (DE-600)2081579-7 1447-0578 nnns volume:15 year:2016 number:4 day:15 month:04 pages:261-265 https://dx.doi.org/10.1007/s12522-016-0242-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 42.23 ASE 44.74 ASE 44.92 ASE AR 15 2016 4 15 04 261-265
allfields_unstemmed	10.1007/s12522-016-0242-z doi (DE-627)SPR026013460 (SPR)s12522-016-0242-z-e DE-627 ger DE-627 rakwb eng 610 ASE 42.23 bkl 44.74 bkl 44.92 bkl Honda, Tomoko verfasserin aut A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary. Fibrous dysplasia of bone (dpeaa)DE-He213 McCune–Albright syndrome (dpeaa)DE-He213 Positron-emission tomography (dpeaa)DE-He213 Precocious pseudopuberty (dpeaa)DE-He213 Sexual precocity (dpeaa)DE-He213 Itoh, Fumiko verfasserin aut Nakamura, Kimitoshi verfasserin aut Ohba, Takashi verfasserin aut Katabuchi, Hidetaka verfasserin aut Enthalten in Reproductive medicine and biology Hoboken, NJ : Wiley, 2002 15(2016), 4 vom: 15. Apr., Seite 261-265 (DE-627)349876223 (DE-600)2081579-7 1447-0578 nnns volume:15 year:2016 number:4 day:15 month:04 pages:261-265 https://dx.doi.org/10.1007/s12522-016-0242-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 42.23 ASE 44.74 ASE 44.92 ASE AR 15 2016 4 15 04 261-265
allfieldsGer	10.1007/s12522-016-0242-z doi (DE-627)SPR026013460 (SPR)s12522-016-0242-z-e DE-627 ger DE-627 rakwb eng 610 ASE 42.23 bkl 44.74 bkl 44.92 bkl Honda, Tomoko verfasserin aut A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary. Fibrous dysplasia of bone (dpeaa)DE-He213 McCune–Albright syndrome (dpeaa)DE-He213 Positron-emission tomography (dpeaa)DE-He213 Precocious pseudopuberty (dpeaa)DE-He213 Sexual precocity (dpeaa)DE-He213 Itoh, Fumiko verfasserin aut Nakamura, Kimitoshi verfasserin aut Ohba, Takashi verfasserin aut Katabuchi, Hidetaka verfasserin aut Enthalten in Reproductive medicine and biology Hoboken, NJ : Wiley, 2002 15(2016), 4 vom: 15. Apr., Seite 261-265 (DE-627)349876223 (DE-600)2081579-7 1447-0578 nnns volume:15 year:2016 number:4 day:15 month:04 pages:261-265 https://dx.doi.org/10.1007/s12522-016-0242-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 42.23 ASE 44.74 ASE 44.92 ASE AR 15 2016 4 15 04 261-265
allfieldsSound	10.1007/s12522-016-0242-z doi (DE-627)SPR026013460 (SPR)s12522-016-0242-z-e DE-627 ger DE-627 rakwb eng 610 ASE 42.23 bkl 44.74 bkl 44.92 bkl Honda, Tomoko verfasserin aut A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary. Fibrous dysplasia of bone (dpeaa)DE-He213 McCune–Albright syndrome (dpeaa)DE-He213 Positron-emission tomography (dpeaa)DE-He213 Precocious pseudopuberty (dpeaa)DE-He213 Sexual precocity (dpeaa)DE-He213 Itoh, Fumiko verfasserin aut Nakamura, Kimitoshi verfasserin aut Ohba, Takashi verfasserin aut Katabuchi, Hidetaka verfasserin aut Enthalten in Reproductive medicine and biology Hoboken, NJ : Wiley, 2002 15(2016), 4 vom: 15. Apr., Seite 261-265 (DE-627)349876223 (DE-600)2081579-7 1447-0578 nnns volume:15 year:2016 number:4 day:15 month:04 pages:261-265 https://dx.doi.org/10.1007/s12522-016-0242-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 42.23 ASE 44.74 ASE 44.92 ASE AR 15 2016 4 15 04 261-265
language	English
source	Enthalten in Reproductive medicine and biology 15(2016), 4 vom: 15. Apr., Seite 261-265 volume:15 year:2016 number:4 day:15 month:04 pages:261-265
sourceStr	Enthalten in Reproductive medicine and biology 15(2016), 4 vom: 15. Apr., Seite 261-265 volume:15 year:2016 number:4 day:15 month:04 pages:261-265
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Fibrous dysplasia of bone McCune–Albright syndrome Positron-emission tomography Precocious pseudopuberty Sexual precocity
dewey-raw	610
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container_title	Reproductive medicine and biology
authorswithroles_txt_mv	Honda, Tomoko @@aut@@ Itoh, Fumiko @@aut@@ Nakamura, Kimitoshi @@aut@@ Ohba, Takashi @@aut@@ Katabuchi, Hidetaka @@aut@@
publishDateDaySort_date	2016-04-15T00:00:00Z
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id	SPR026013460
language_de	englisch
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author	Honda, Tomoko
spellingShingle	Honda, Tomoko ddc 610 bkl 42.23 bkl 44.74 bkl 44.92 misc Fibrous dysplasia of bone misc McCune–Albright syndrome misc Positron-emission tomography misc Precocious pseudopuberty misc Sexual precocity A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up
authorStr	Honda, Tomoko
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topic_title	610 ASE 42.23 bkl 44.74 bkl 44.92 bkl A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up Fibrous dysplasia of bone (dpeaa)DE-He213 McCune–Albright syndrome (dpeaa)DE-He213 Positron-emission tomography (dpeaa)DE-He213 Precocious pseudopuberty (dpeaa)DE-He213 Sexual precocity (dpeaa)DE-He213
topic	ddc 610 bkl 42.23 bkl 44.74 bkl 44.92 misc Fibrous dysplasia of bone misc McCune–Albright syndrome misc Positron-emission tomography misc Precocious pseudopuberty misc Sexual precocity
topic_unstemmed	ddc 610 bkl 42.23 bkl 44.74 bkl 44.92 misc Fibrous dysplasia of bone misc McCune–Albright syndrome misc Positron-emission tomography misc Precocious pseudopuberty misc Sexual precocity
topic_browse	ddc 610 bkl 42.23 bkl 44.74 bkl 44.92 misc Fibrous dysplasia of bone misc McCune–Albright syndrome misc Positron-emission tomography misc Precocious pseudopuberty misc Sexual precocity
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title	A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up
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title_full	A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up
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author_browse	Honda, Tomoko Itoh, Fumiko Nakamura, Kimitoshi Ohba, Takashi Katabuchi, Hidetaka
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title_sort	case of gradually manifesting mccune–albright syndrome with a 10-year follow-up
title_auth	A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up
abstract	Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary.
abstractGer	Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary.
abstract_unstemmed	Abstract McCune–Albright syndrome (MAS) is characterized by fibrous dysplasia (FD) of bone, café-au-lait skin pigmentation, and precocious puberty. Here we report a case of a 12-year-old girl with MAS presenting sexual precocity as initial signs, followed by FD of bone with her growth. She was referred to our hospital because of breast budding and abnormal genital bleeding at the age of 2.8 years. On physical examination, her height and weight were greater than two standard deviations of the mean ranges. Hormonal analysis revealed an elevated serum estradiol and suppressed luteinizing hormone and follicle-stimulating hormone production. Her bone age had advanced, and a 16-mm monocystic lesion was observed on her right ovary by pelvic ultrasonography. Considering the clinical and paraclinical findings, precocious pseudopuberty was suspected and periodic observations were started. Her estrogen “flare up” was transient and she had repeated similar episodes three times in the following 7 years. She complained of pain in her right hip at the age of 9.6 years, which was diagnosed as FD of bone by fluorodeoxyglucose-positron emission tomography. Although no café-au-lait skin pigmentation was observed, we made a preliminary diagnosis of MAS. Because clinical evidence for MAS can appear later in the course of recurrent autonomous cysts, careful observation and periodical assessments of patients with suspected MAS is necessary.
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container_issue	4
title_short	A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up
url	https://dx.doi.org/10.1007/s12522-016-0242-z
remote_bool	true
author2	Itoh, Fumiko Nakamura, Kimitoshi Ohba, Takashi Katabuchi, Hidetaka
author2Str	Itoh, Fumiko Nakamura, Kimitoshi Ohba, Takashi Katabuchi, Hidetaka
ppnlink	349876223
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doi_str	10.1007/s12522-016-0242-z
up_date	2024-07-03T18:20:57.748Z
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A case of gradually manifesting McCune–Albright syndrome with a 10-year follow-up

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