- Histopathological Observation of Cafe au Lait Spots
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Choi SJ, Yu HJ, Sohn SJ
- KMID: 1679593
- Korean J Dermatol.
- 1986 Aug;24(4):506-509.
We observed 17 cases of cafe au lait spots histopathplogi ally. Out of 17 cases, 9 cases were neurofibromatosis with neurofibromas, 6 cases were neurofibromatosis without neurofibroma, and 2 cases... -
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- A Case of Multiple Cafe-au-lait Spots with Nevus Depigmentosus and Hemangioma
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Ko JY, Ro YS, Lee CW, Kim JH
- KMID: 2086598
- Korean J Dermatol.
- 2002 Oct;40(10):1253-1255.
When 6 or more Cafe-au-lait spots(CALS) tend to be randomly and widely distributed, we must rule out neurofibromatosis(NF). Nevus depigmentosus is a congenital nonprogressive hypopigmented patch that shows histologically decreased... -
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- Congenital Café-au-Lait Spot and Sequentially Occurred Nevus Spilus
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Kim JY, Lee ES
- KMID: 2158544
- Ann Dermatol.
- 2004 Dec;16(4):191-193.
- doi: 10.5021/ad.2004.16.4.191
No abstract available. -
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- A Case of Segmental Neurofibromatosis
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Choi GS, Lee J, Won DH, Koo SW, Lee JH, Kim YK
- KMID: 2359744
- Ann Dermatol.
- 1999 Apr;11(2):109-111.
- doi: 10.5021/ad.1999.11.2.109
Segmental neurofibromatosis is a rare disorder characterized by cafe-au-lait spots and neurofibrobmas, or only neurofibroma, limited to one region of the body. Disease-associated systemic involvement is uncommon. Most patients with... -
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- A Case of Juvenile Xanthogranuloma Associated with Juvenile Chronic Myeloid Leukemia and Neurofibromatosis
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Roh JY, Park HJ, Cinn YW, Kim SN, Kim SG
- KMID: 2146587
- Korean J Dermatol.
- 1987 Jun;25(3):404-409.
Juvenile xanthogranuloma(JXG) is a a benign histiocytic proliferative disorder most frequently seen in infants. The usual course is self-limited, but it may be a manifestation of juvenile chronic myeloid leukemia(JCML).... -
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- A Case Congenital Pseudarthrosis of Tibia
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Yoon TH, Shin YH, Kim OS
- KMID: 2460265
- J Korean Orthop Assoc.
- 1979 Dec;14(4):648-652.
- doi: 10.4055/jkoa.1979.14.4.648
Congenital pseudarthrosis of the tibia is a condition most often combined with cafe-au-lait spots and neurofibromatosis. It is notoriously difficult to attain a sound bony union. Compression plating and screw... -
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- Two Cases of Segmental Neurofibromatosis
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Cho CG, Kim IH, Song HJ, Oh CH
- KMID: 2230540
- Korean J Dermatol.
- 1998 Dec;36(6):1083-1087.
Neurofibromatosis(NF) is a disorder characterized by its relative commonness, variability, and heterogeneity. It is usually expressed as a generalized form, but is rarely localized in a limited part of the... -
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- Isodicentric Chromosome 15 Syndrome in a Korean Patient With Cafe-au-lait Spots
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Rim JH, Chung HJ, Shin S, Park SJ, Choi JR
- KMID: 2045876
- Ann Lab Med.
- 2015 Jul;35(4):474-476.
- doi: 10.3343/alm.2015.35.4.474
No abstract available. -
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- Treatment of Hyperpigmented Disease with 4-Isopropylcatechol
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Byun DG, Kim JH, Park YJ, Lee SB
- KMID: 1664483
- Korean J Dermatol.
- 1975 Mar;13(1):5-7.
Disfiguring hyperpigmentation of the exposed areas may have impartant and lasting effects on the emotional well-being of the patient. And many attempts to treat areas of hyperpigmentation have been earried... -
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- A Case of Radiologically Suspected Mesenteric Plexiform Neurofibromas in a Patient with Type I Neurofibromatosis
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Oh SM, Kim YO, Son YJ, Woo YJ
- KMID: 2329433
- J Korean Child Neurol Soc.
- 2009 Nov;17(2):226-230.
Neurofibromatosis type I(NF-1) is an autosomal dominant neurocutaneous syndrome characterized by cafe-au-lait spots, optic glioma, skeletal dysplasia, and iris hamartoma. Mesenteric plexiform neurofibromas(PNF) have been rarely reported in NF-1, especially... -
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- A Case of Eyelid Neurofibroma in yon Recklinghausen's Disease
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Hah MC, Han YJ, Hong SH
- KMID: 2336356
- J Korean Ophthalmol Soc.
- 1974 Dec;15(4):361-363.
We experienced a case of eyelid neurofibroma in von Recklinghausen's disease, which had a typical sign, cafe-au-lait spots on generalized skin. The patient was a five year old girl who... -
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- MULTIPLE NEUROFIBROMATOSIS WITH ORAL, PARAPHARYNGEAL SPACE AND WHOLE BODY LESIONS
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Oh SS, Hwang HJ, Kim IK, Cho JH, Kim HD, On NS, Park EJ
- KMID: 1961353
- J Korean Assoc Oral Maxillofac Surg.
- 1999 Apr;25(2):178-181.
Neurofibromatosis(Von Recklinghausen's disease) is an autosomal dominant disease that affects one in 2,500-3,000 births. The clinical presentation is characterized by multiple pigmented lesions of the skin, known as cafe-au-lait spots,... -
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- Neurofibromatosis Type 1 with Cerebellar Piloytic Astrocytoma
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Jeon IS, Kim JS, Kim JH, Kim NR
- KMID: 1654707
- Korean J Pediatr.
- 2004 Apr;47(4):458-461.
Neurofibromatosis type 1(NF1) is one of the most common inherited disorders, clinically characterized by cafe-au-lait spots, Lisch nodules and neurofibromas. In addition, the affected individuals usually develop benign and malignant... -
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- A Case of Juvenile Xanthogranuloma Associated with Neurofibromatosis
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Kye YC, Choi HC, Oh CH, Kim SN
- KMID: 2361729
- Ann Dermatol.
- 1993 Jan;5(1):22-24.
- doi: 10.5021/ad.1993.5.1.22
We report a case of juvenile xanthogranuloma associated with neurofibromatosis. The patient was a 10-month-old female who had multiple yellowish papules on the face and shoulders A Biopsy of these... -
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- Congenital Pseudarthrosis associated with Neurofibromatosis: A case report
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Lee EW, Kang JW, Lee CH, Yoon WS, Kim JC
- KMID: 2461803
- J Korean Orthop Assoc.
- 1977 Sep;12(3):517-522.
- doi: 10.4055/jkoa.1977.12.3.517
Congenital pseudarthrosis is frequently associated with various stigmata of neurofibromatosis, particularly Cafe-Au-Lait spots and,subcutaneous nodules and in these patients, it is noteworthy that the treatment is very difficult even with... -
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- Congenital Pseudarthrosis of the Tibia: 5 Cases Report
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Kim NH, Kang SY
- KMID: 2457842
- J Korean Orthop Assoc.
- 1982 Oct;17(5):988-994.
- doi: 10.4055/jkoa.1982.17.5.988
Five cases of congenital pseuduthrosis of the tibia were treated at Department of Orthopedic Surgery, Yonsei Medical Center from September 1971 to February 1982. In four cases, many cafe-au-lait spots... -
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- A Case of Segmental Neurofibromatosis
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Lee TK, Moon DC, Kwon KS, Chung TA
- KMID: 2231451
- Korean J Dermatol.
- 1987 Oct;25(5):696-699.
A 61-year-old female had neurofibromas situated on the right side of upper trunk, shoulder and neck in the distribution of dermatomes C3 and C4(right), which developed 3 years ago.... -
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- A Case of Eccrine Spiradenoma in a Neurofibromatosis Type-1 Patient
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Choi JH, Lee HB, Park CK, Kim HO, Park CW, Lee CH
- KMID: 1771551
- Korean J Dermatol.
- 2008 Aug;46(8):1087-1089.
Eccrine spiradenoma is a rare benign tumor which is differentiated into the direction of eccrine gland. Neurofibromatosis type-1 is an autosomal dominantly inherited disorder that is characterized by neurofibroma, cafe... -
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- A Case of Epidermal Nevus Syndrome
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Ahn SK, Hann SK, Lee SH, Lee S
- KMID: 2362004
- Ann Dermatol.
- 1991 Jul;3(2):126-129.
- doi: 10.5021/ad.1991.3.2.126
We report a case of epidermal nevus syndrome. The patient was a 26-year-old female who had numerous linear verrucous plaques on her neck, upper back and anterior chest. Biopsy of... -
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- A Case fo Elephantiasis Neuromatosa
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Kim SK, Kim TJ, Yang SK, Kim JT
- KMID: 1678140
- Korean J Dermatol.
- 1980 Dec;18(6):613-617.
Elephantiasis neuromatosa is one of 3 types of cutaneous tumors in Von Recklinghausen's disease. This 28 year-old male patient visited for adult-fist sized tumor associated with hairy pigmented patch on... -
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