본문 바로가기
KERD
논문KCI 등재

Clinical and radiological features of pituitary stalk lesions in children and adolescents

2

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류소아과학

초록

Purpose: The diagnosis of pituitary stalk lesion has been based on clinical feature, radiologic assessment for its critical location and role. This study aimed to investigate clinical symptoms, endocrine disturbance, magnetic resonance imaging (MRI) findings of pituitary stalk lesions in children and adolescents and to evaluate differences between neoplastic lesions with the others. Methods: We performed a retrospective review of patients under 18 years old with pituitary stalk lesions diagnosed at the Seoul National University Children’s Hospital between 2000 and 2013, by a text search for head MRI reports by using 'pituitary stalk', 'infundibulum', and 'infundibular stalk', as keywords. Results: For the 76 patients, sixteen patients (21.1%) had congenital lesions, and 52 (68.4%) had neoplasms. No inflammatory lesions were found. Diabetes insipidus (DI) was the most common endocrine defect, diagnosed in 38 patients (50%). There was male predominance especially in neoplastic group. Thickened pituitary stalk was, but enhancement of lesion was not, associated with neoplasm. DI was more prevalent in neoplastic stalk lesions. Anterior pituitary dysfunction such as growth hormone and adrenocorticotropic hormone deficiencies were less prevalent in neoplastic lesions of pituitary stalk. Conclusion: In conclusion, the etiology of pituitary stalk lesions in children and adolescents is diverse and different from that in adults. Neoplastic pituitary stalk lesions can be differentiated from nonneoplastic lesions by systemic evaluation of clinical, hormonal, radiological findings.

Abstract

Purpose: The diagnosis of pituitary stalk lesion has been based on clinical feature, radiologic assessment for its critical location and role. This study aimed to investigate clinical symptoms, endocrine disturbance, magnetic resonance imaging (MRI) findings of pituitary stalk lesions in children and adolescents and to evaluate differences between neoplastic lesions with the others. Methods: We performed a retrospective review of patients under 18 years old with pituitary stalk lesions diagnosed at the Seoul National University Children’s Hospital between 2000 and 2013, by a text search for head MRI reports by using 'pituitary stalk', 'infundibulum', and 'infundibular stalk', as keywords. Results: For the 76 patients, sixteen patients (21.1%) had congenital lesions, and 52 (68.4%) had neoplasms. No inflammatory lesions were found. Diabetes insipidus (DI) was the most common endocrine defect, diagnosed in 38 patients (50%). There was male predominance especially in neoplastic group. Thickened pituitary stalk was, but enhancement of lesion was not, associated with neoplasm. DI was more prevalent in neoplastic stalk lesions. Anterior pituitary dysfunction such as growth hormone and adrenocorticotropic hormone deficiencies were less prevalent in neoplastic lesions of pituitary stalk. Conclusion: In conclusion, the etiology of pituitary stalk lesions in children and adolescents is diverse and different from that in adults. Neoplastic pituitary stalk lesions can be differentiated from nonneoplastic lesions by systemic evaluation of clinical, hormonal, radiological findings.

참고문헌 (16)

  1. Simmons GE, "MR imaging of the pituitary stalk: size, shape, and enhancement pattern", AJR Am J Roentgenol, 159, pp.375~377 (1992)
  2. Rupp D, "Pituitary stalk lesions", Curr Opin Endocrinol Diabetes Obes, 15, pp.339~345 (2008)
  3. Turcu AF, "Pituitary stalk lesions: the Mayo Clinic experience", J Clin Endocrinol Metab, 98, pp.1812~1818 (2013)
  4. Hamilton BE, "Anatomic and pathologic spectrum of pituitary infundibulum lesions", AJR Am J Roentgenol, 188, pp.W223~W232 (2007)
  5. Marchand I, "Central diabetes insipidus as the inaugural manifestation of Langerhans cell histiocytosis:natural history and medical evaluation of 26 children and adolescents", J Clin Endocrinol Metab, 96, pp.E1352~E1360 (2011)
  6. Di Iorgi N, "Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases", J Clin Endocrinol Metab, 99, pp.1264~1272 (2014)
  7. Beni-Adani L, "Surgical implications of the thickened pituitary stalk accompanied by central diabetes insipidus", J Neurosurg, 103(2 Suppl), pp.142~147 (2005)
  8. Bihan H, "Sarcoidosis: clinical, hormonal, and magnetic resonance imaging (MRI) manifestations of hypothalamicpituitary disease in 9 patients and review of the literature", Medicine, 86, pp.259~268 (2007)
  9. Twilt M, "Childhood inflammatory brain diseases: pathogenesis, diagnosis and therapy", Rheumatology, 53, pp.1359~1368 (2014)
  10. Nozaki K, "Isolated neurosarcoidosis: case series in 2 sarcoidosis centers", Neurologist, 18, pp.373~377 (2012)
  11. Oksanen V, "Neurosarcoidosis: clinical presentations and course in 50 patients", Acta Neurol Scand, 73, pp.283~290 (1986)
  12. Iannuzzi MC, "Sarcoidosis", N Engl J Med, 357, pp.2153~2165 (2007)
  13. Pietinalho A, "The frequency of sarcoidosis in Finland and Hokkaido, Japan. A comparative epidemiological study", Sarcoidosis, 12, pp.61~67 (1995)
  14. Scholten V, "An unusual presentation of neurosarcoidosis in an 11-year-old boy", Can J Neurol Sci, 36, pp.783~786 (2009)
  15. Tsao CY, "Isolated neurosarcoidosis presenting as headache and multiple brain and spinal cord lesions mimicking central nervous system metastases", Brain Dev, 29, pp.514~518 (2007)
  16. Baumann RJ, "Neurosarcoid presents differently in children than in adults", Pediatrics, 112(6Pt 1), pp.e480~e486 (2003)

관련 논문AI추천

Clinical and radiological findings of incidental Rathke’s cleft cysts in children and adolescents양승, 박홍규, 송준호, 오연정, 황일태대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2014 · 제19권 제1호Clinical manifestations of Rathke’s cleft cysts and their natural progression during 2 years in children and adolescents권아름, 김덕희, 김호성, 정모경, 조은정, 진주현, 채현욱대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2017 · 제22권 제3호Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency고철우, 장경미대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2017 · 제22권 제3호Pituitary abnormalities in patients with pediatric growth hormone deficiency in a single tertiary centerJung Hyeon Jun, Kim Jeong Rye, Yu Jeesuk대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2024 · 제29권 제6호소아 청소년기에 발생한 뇌하수체 선종 24 증례의 임상상과 치료경과김화영, 신충호, 양세원, 윤주영, 이영아, 이지은, 정혜운대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2012 · 제17권 제2호Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort studyKo Jung Min, Lee Yoonha, Lee Young Ah, Lee Yun Jeong, Shin Choong Ho대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2024 · 제29권 제6호

이 간행물의 다른 논문 (9건)