1.Congenital Café-au-Lait Spot and Sequentially Occurred Nevus Spilus.
Annals of Dermatology 2004;16(4):191-193
No abstract available.
Cafe-au-Lait Spots
;
Nevus*
2.Treatment of Hyperpigmented Disease with 4-Isopropylcatechol.
Dong Gil BYUN ; Joung Hoe KIM ; Yang Ja PARK ; Soon Bok LEE
Korean Journal of Dermatology 1975;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 out, but all of them are not very successful. Recently 4-isopropylcatechol has been known to inhibit melanin pigmentation with a selective action on melanocytes either destroying or inactivating the melanocytes experimentally. There is no report on its clinical trial till now. In this study, 1% 4-isopropylcatechol cream was topieally applied to the hyperpigmented lesions of 29 patieots of melasma, freckle, and cafe-au-lait spot. The bleaching effect on meiasmas was very satisfactory in all patients but coantact dermatltis in 3 patients and reticular hyperpigmentation with areas of depigmented spots in one patient were developed as the side effects of the drug. Freckle and cafe-au-Iait spots were not bleached.
Cafe-au-Lait Spots
;
Humans
;
Hyperpigmentation
;
Melanins
;
Melanocytes
;
Melanosis
;
Pigmentation
3.Isodicentric Chromosome 15 Syndrome in a Korean Patient With Cafe-au-lait Spots.
John Hoon RIM ; Hee Jung CHUNG ; Saeam SHIN ; Seo Jin PARK ; Jong Rak CHOI
Annals of Laboratory Medicine 2015;35(4):474-476
No abstract available.
Cafe-au-Lait Spots*
;
Chromosomes, Human, Pair 15*
;
Humans
4.Histopathological Observation of Cafe au Lait Spots.
Sung Jun CHOI ; Hee Joon YU ; Sook Ja SOHN
Korean Journal of Dermatology 1986;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 were normal healthy persons. The results were as follows. l. In all 17 cases, melanin pigment was increased in melanocytes and keratinocytes. 2. Griant pigment granules were identified only in 3 cases of neurofibromatosis with neurofibromas.
Cafe-au-Lait Spots*
;
Humans
;
Keratinocytes
;
Melanins
;
Melanocytes
;
Neurofibroma
;
Neurofibromatoses
5.A Case Congenital Pseudarthrosis of Tibia
Te Hyun YOON ; Young Hwan SHIN ; Ok Suck KIM
The Journal of the Korean Orthopaedic Association 1979;14(4):648-652
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 fixation with massive bone graft resulted in successful union in our case.
Cafe-au-Lait Spots
;
Neurofibromatoses
;
Pseudarthrosis
;
Tibia
;
Transplants
6.A Case of Segmental Neurofibromatosis.
Chan Seok OH ; Jae Wook MYUNG ; Hye Jin WOO ; Sang Hyun CHO
Korean Journal of Dermatology 2002;40(7):832-834
A 30-year-old woman had localized several cutaneous neurofibromas on the scalp in a dermatomal distribution(C2). Family history was negative, and evaluation for other signs such as cafe-au-lait spots, axillary frecklings, or Lisch nodules were not revealed. Biopsy specimen showed a well-circumscribed encapsulated tumor which consists of spindle cells with elongated, wavy nuclei and thin wavy collagenous strands loosely spaced in a clear matrix as seen in the neurofibroma. The diagnosis of bilateral segmental neurofibromatosis was made on the basis of the clinical features including the distribution of the neurofibromas and the absence of the family history and the histology consistent with a neurofibroma.
Adult
;
Biopsy
;
Cafe-au-Lait Spots
;
Collagen
;
Diagnosis
;
Female
;
Humans
;
Neurofibroma
;
Neurofibromatoses*
;
Scalp
7.A Case of Multiple Cafe-au-lait Spots with Nevus Depigmentosus and Hemangioma.
Joo Youn KO ; Young Suck RO ; Chang Woo LEE ; Jae Hong KIM
Korean Journal of Dermatology 2002;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 pigmentation while CALS shows increased pigmentation. We report a case of a 16-month-old girl showing generalized multiple cafe-au-lait spots with segmental nevus depigmentosus and capillary hemangioma on her right upper back. A possible explanation for the co-occurrence of CALS and nevus depigmentosus could be the concept of mosaicism.
Cafe-au-Lait Spots*
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Female
;
Hemangioma*
;
Hemangioma, Capillary
;
Humans
;
Infant
;
Mosaicism
;
Nevus*
;
Pigmentation
8.A Case of Segmental Neurofibromatosis.
Jin Hyouk CHOI ; Soon Wook KWON ; Moo Kyu SUH ; Ho Chung LEE ; Sung Wook LIM ; Jeong Woo LEE ; Jung Ran KIM
Korean Journal of Dermatology 2003;41(6):820-822
Segmental neurofibromatosis(neurofibromatosis type V) is rare disorder characterized by limitation of cafe-au-lait spots and neurofibroma or only neurofibroma on a given unilateral segment of the body. We report a case of segmental neurofibromatosis that developed in a 58-year-old male. The skin lesion was situated on the right antecubital area and wrist in the distribution of dermatomes C5 and C6. Histopathologic examination showed well-demarcated, non-encapsulated tumor of the dermis was composed of thin wavy collagenous fibers and loosely spaced spindle cells with elongated wavy nuclei. The patient was treated with surgical excision and carbon dioxide laser.
Cafe-au-Lait Spots
;
Collagen
;
Dermis
;
Humans
;
Lasers, Gas
;
Male
;
Middle Aged
;
Neurofibroma
;
Neurofibromatoses*
;
Skin
;
Wrist
9.Two Cases of Plexiform Neurilemmoma.
Sung Eun CHANG ; Yeon Soon LIM ; Jee Ho CHOI ; Kyung Jeh SUNG ; Kee Chan MOON ; Jai Kyoung KOH
Korean Journal of Dermatology 1999;37(4):510-513
Plexiform neurilemmoma is a relatively rare, benign peripheral nerve sheath tumor, whieh usually arises in either the dermis or subcutaneous tissue. These tumors may occur singly or as multiple lesions (plexiform neurilemmomatosis), We report an unusual case of plexiform neurilemmomatosis associated with cafe au lait spots reminiscent of neurofibromatosis clinically and another case of plexiform neurilemmoma on the finger. A Biopsy revealed the characteristic palisaded arrangement of spindle cells within well circumscribed elongated nodules, The skin lesions were completely excised without recurrence thereafter.
Biopsy
;
Cafe-au-Lait Spots
;
Dermis
;
Fingers
;
Neurilemmoma*
;
Neurofibromatoses
;
Peripheral Nerves
;
Recurrence
;
Skin
;
Subcutaneous Tissue
10.Retroperitoneal Malignant Peripheral Nerve Sheath Tumors Complicated with Type I Neurofibromatosis.
Bonuk GU ; Jin Woo PARK ; Lee Chan JANG ; Seok Hyung KIM ; Il Hun BAE ; Woo Yoon PARK ; Seung Tak KIM
Journal of the Korean Surgical Society 2006;71(5):365-370
Neurofibromatosis is an infrequent genetic disorder that was first clinically described by von Recklinghausen and it was classified into 7 types by Riccardi. Type I neurofibromatosis is the most common type, and it is characterized by neurofibromas of variable size and multiple cafe-au-lait spots with minimal CNS lesion, if any. Malignant tumors develop in 2 to 13% of patients with type I neurofibromatosis, but they are rarely found in the retroperitoneum. We surgically resected huge retroperitoneal malignant peripheral nerve sheath tumors in 2 patients with sporadic type I neurofibromatosis. One patient survived 10 months and the other survived 3 months after operation. Retroperitoneal malignant peripheral nerve sheath tumor shows a poor prognosis even after surgical resection because of frequent recurrence and the lack of effective adjuvant therapy. Early diagnosis and development of new adjuvant therapy are required to effectively treat this malady.
Cafe-au-Lait Spots
;
Early Diagnosis
;
Humans
;
Neurilemmoma*
;
Neurofibroma
;
Neurofibromatoses*
;
Neurofibromatosis 1
;
Peripheral Nerves
;
Prognosis
;
Recurrence