- Breast Gigantism Induced by D-Penicillamine: Case Report
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Cha JH, Kim HH, Kim SM, Seo MH, Yoon HS
- KMID: 2199851
- J Korean Radiol Soc.
- 2004 Mar;50(3):213-215.
- doi: 10.3348/jkrs.2004.50.3.213
D-penicillamine, a chelating agent of copper, is the drug of choice for the treatment of Wilson's disease. Breast enlargement is a rare complication arising from its use, and we report... -
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- A Case of Klinefelter Syndrome Differentially Diagnosed as a Cause of Gigantism
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Kim JY, Choi YJ, Rhee SY
- KMID: 2259004
- Korean J Med.
- 2011 Mar;80(3):343-347.
Klinefelter syndrome is a congenital disease that is associated with the existence of an extra X chromosome, and is one of the most common causes of male primary hypogonadism. In... -
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- Klippel-trenaunay-weber syndrome
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Ryu KN, Lee SW, Yoon Y, Lim JH
- KMID: 2358829
- J Korean Radiol Soc.
- 1990 Oct;26(5):1053-1056.
- doi: 10.3348/jkrs.1990.26.5.1053
The Klippel-Trenaunay-Weber syndrome is characterized by a classical triad that includes unilateral cutaneouscapillary hemangiomas, varicose veins, and local gigantism with both soft tissue and osseous overgrowth. Authorshave experienced one case... -
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- A Case of Beckwith Syndrome
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Kim KT, Hong DS, Nam BD, Kim KT
- KMID: 1946088
- J Korean Pediatr Soc.
- 1981 Jul;24(7):696-698.
We experienced one case of Beckwith syndrome. This one day aged male neonate manifested macroglossia, umbilical hernia, visceromegaly, hypoglycemia, gigantism and polycythemia. A brief review of related literature is also... -
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- A case of Breast Gigantism in a Patient with Wilson's Disease treated by Penicillamine
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Lee JE, Shin HJ, Hwang SE, Hwang KT, Oh SK, Youn YK, Noh DY, Kim SW, Han W
- KMID: 1976172
- J Breast Cancer.
- 2006 Mar;9(1):69-72.
- doi: 10.4048/jbc.2006.9.1.69
We report a case of breast gigantism in a patient with Wilson's disease treated with penicillamine. A 19-year-old female with alleged Wilson's disease visited our hospital due to diffuse enlargement... -
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- A Case of Macrodactyly
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Jung M, Chung CH
- KMID: 2471605
- J Korean Orthop Assoc.
- 1974 Mar;9(1):96-98.
- doi: 10.4055/jkoa.1974.9.1.96
Macrodactyly is a rare congenital malformation characterized by an increase in the size of all the elements or structures of digit or digits. The phalanges, tendons, nerves, vessels, subcutaneous fat,... -
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- Microsurgical Transsphenoidal Approach for Pituitary Denomas
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Hahn YS, Lee HJ
- KMID: 2106967
- J Korean Neurosurg Soc.
- 1976 Oct;5(2):195-208.
3 cases of pituitary adenomas, two hormone-secreting adenomas, and one non-secreting chromophobe adenoma, were treated surgically by the sublabial transsphenoidal approach with use of surgical microscope and radiofluroscopic image intensification... -
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- Gigantism caused by growth hormone secreting pituitary adenoma
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Rhee N, Jeong K, Yang EM, Kim CJ
- KMID: 1803861
- Ann Pediatr Endocrinol Metab.
- 2014 Jun;19(2):96-99.
- doi: 10.6065/apem.2014.19.2.96
Gigantism indicates excessive secretion of growth hormones (GH) during childhood when open epiphyseal growth plates allow for excessive linear growth. Case one involved a 14.7-year-old boy presented with extreme tall... -
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- Primary hyperparathyroidism erosion of the sternal ends of the clavicles, a new sign of hyperparathy...
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Chae IW, Rhee BC
- KMID: 2345655
- J Korean Radiol Soc.
- 1975 Sep;11(2):159-165.
- doi: 10.3348/jkrs.1975.11.2.159
A Radiological analysis was made of 13 cases of confirmed acromegaly and gigantism. And observation was madein skeleton and soft tissue of patients at Yonsei university from 1968 to 1973.... -
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- Testicular Yolk Sac Tumor in Beckwith-Wiedemann Syndrome
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Park BJ, Jeong IY, Ro DW, Kim DY, Park JS
- KMID: 1663291
- Korean J Urol.
- 1996 Dec;37(12):1417-1420.
The Beckwith-Wiedemann syndrome, which included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, have a substantially increased risk for the development of tumor. We report a case of testicular... -
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- Radiologic Imaging Findings of Bilateral Infiltrating Pseudoangiomatous Stromal Hyperplasia of the Breasts: A Case Report
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Go HS, Jeh SK
- KMID: 1425149
- J Korean Soc Radiol.
- 2013 Apr;68(4):329-332.
- doi: 10.3348/jksr.2013.68.4.329
Pseudoangiomatous stromal hyperplasia (PASH), first described by Vuitch et al., is a rare benign lesion, shows the proliferation of the breast stromal tissue. We experienced a case of a 19-year-old... -
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- Hypertrophy of an Extremity Associated with Neurofibromatosis of the Sural Nerve: Report of one case
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Kim ID, Lee SY, Ihin JC, Park YC
- KMID: 2461802
- J Korean Orthop Assoc.
- 1977 Sep;12(3):513-516.
- doi: 10.4055/jkoa.1977.12.3.513
Overgrowth and hypertrophy of one or more extremities is an infrequentIy encountered congenital or acguired anomaly, It is referred to in the literature by different authors as local gigantism, hypertrophy... -
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- Management of Proteus Syndrome with Craniofacial Hemihyperostosis: Case Report
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Yun YE, Seol KY, Oh MS, Choi JG, Kim SJ, Lee DK, Kang JY
- KMID: 2136938
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 2011 Nov;33(6):540-548.
Proteus syndrome is a congenital hamartomatous malformation that is characterized by a wide range of deformities, including craniofacial deformities. Proteus syndrome features partial gigantism and asymmetry of the limbs, plantar... -
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- Reduction glossectomy of macroglossia in beckwith-wiedemann syndrome : a case report
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Kim HK, Kim ES, Ko YK, Kim SG
- KMID: 1575609
- J Korean Assoc Maxillofac Plast Reconstr Surg.
- 2005 Nov;27(6):559-564.
Beckwith-Wiedemann syndrome is an autosomal dominant growth excess disorder, which occurs with a reported incidence of 1 in 13,700 to 1 in 17,000 live births. It constitutes a discrete... -
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- A CASE OF TONGUE RESECTION IN MACROGLOSSIA AS A PRESENTATION OF BECKWITH-WIEDEMANN SYNDROME
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Ahn KY, Jang KS, Park DH, Hwang JB
- KMID: 2119323
- J Korean Soc Plast Reconstr Surg.
- 1997 Jan;24(1):199-204.
The Beckwith-Wiedemann syndrome, originally described by Beckwith in 1963 and Wiedemann in 1964, included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, severe hypoglycemia, abdominal wall defect, capillary nevus... -
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- A Case of Isolated Familial Somatotropinoma
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Park HR, Kim EA, Jiang MH, Jang CS, Lee KW, Hong SB, Kim EY, Lim MK, Nam MS, Kim YS
- KMID: 2200527
- J Korean Soc Endocrinol.
- 2004 Aug;19(4):398-405.
The familial occurrence of a pituitary adenoma associated with multiple endocrine neoplasia (MEN) type 1 or Carney complex is a well-recognized entity. However, an isolated familial somatotropinoma is a rare... -
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- A case of acromegaly associated with moyamoya disease, coronary arterial stenosis, and dilated cardiomyopathy
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Lee DH, Kim YJ, Lee DB, Park JH, Chung DJ, Chung MY, Lee TH
- KMID: 2306240
- Korean J Med.
- 2000 Feb;58(2):227-233.
A 19-year-old girl with typical features of acromegaly, duration of which was thought to be above 10 years, presented with dyspnea. After serial studies, dilated cardiomyopathy and critical stenosis of... -
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- Signature Genes in Macrodactyly through Transcriptome Network Analysis Reveal their Association of Lipid Metabolism
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Choi JW, Lee HJ, Oh JW
- KMID: 2392273
- Korean J Phys Anthropol.
- 2017 Sep;30(3):77-85.
- doi: 10.11637/kjpa.2017.30.3.77
Macrodactyly is one of the most difficult hand anomalies to treat not only surgically but medically as well. Little is known about the molecular pathways and lipid metabolism of this... -
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- Scoliosis in Neurofibromatosis
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Suk SI, Song HS, Chang JS
- KMID: 2457880
- J Korean Orthop Assoc.
- 1982 Apr;17(2):213-221.
- doi: 10.4055/jkoa.1982.17.2.213
Neurofibromatosis is a disease which involves both neuroectodermal and mesodermal tissue, and is characterized by cafe-au-lait spot, multiple subcutaneous neurofibromas, elephantiasis neuromatosa, a positive family history, and specific dystrophic osseous... -
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