- Bullous Annular Erythema as a Cutaneous Sign of Vaginal Stump Adenocarcinoma
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Lee HM, Lee JS, Koo DW
- KMID: 2265994
- Ann Dermatol.
- 2013 Feb;25(1):131-132.
- doi: 10.5021/ad.2013.25.1.131
No abstract available. -
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- A Case of Multiple Osteoma Cutis in Infant
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Park HS, Yun SJ, Kim SJ, Lee SC, Won YH, Lee JB
- KMID: 2088506
- Korean J Dermatol.
- 2012 Oct;50(10):921-922.
No abstract available. -
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- A Case of Perforating Osteoma Cutis
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Cho HH, Ko HC, Kim SJ, Kim MB, Kwon KS, Oh CK
- KMID: 2302115
- Korean J Dermatol.
- 2008 Feb;46(2):249-251.
Among skin disorders associated with changes to the bony tissue or abnormalities of calcification, osteoma cutis is a rare, benign tumor of the skin composed of compact bone. Osteoma cutis... -
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- A Case of Miliary Osteoma Cutis on the Jaw
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Cho SB, Lee SJ, Oh SW, Lee SH, Oh SH
- KMID: 2302125
- Korean J Dermatol.
- 2008 Feb;46(2):289-291.
Miliary osteoma cutis of the face is a form of primary osteoma cutis. We report a case of miliary osteoma cutis on the jaw of a 55-year-old female. She presented... -
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- A Case of Idiopathic Eruptive Macular Pigmentation Limited to Flexural Areas
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Kim EH, Lee ES, Kim YC, Kang HY
- KMID: 2172094
- Ann Dermatol.
- 2008 Jun;20(2):98-101.
- doi: 10.5021/ad.2008.20.2.98
Idiopathic eruptive macular pigmentation is a rare condition characterized by asymptomatic pigmented macules involving the neck, trunk, and proximal portions of the extremities. On histopathologic examination, there was increased pigmentation... -
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- Miliary Osteoma Cutis of the Face in Middle-aged Women
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Choi KC, Song IG, Na CH, Shin BS
- KMID: 2301867
- Korean J Dermatol.
- 2010 Jul;48(7):586-589.
Miliary osteoma cutis of the face is a variant of osteoma cutis, and this malady occurs in middle-aged to older women with or without a previous history of acne vulgaris.... -
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- A Case of Becker's Nevus with Osteoma Cutis
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Park SB, Song BH, Park EJ, Kwon IH, Kim KH, Kim KJ
- KMID: 2156801
- Ann Dermatol.
- 2011 Oct;23(Suppl 2):S247-S249.
- doi: 10.5021/ad.2011.23.S2.S247
Becker's nevus is a relatively common acquired focal epidermal melanotic hypermelanosis usually found in the region of the shoulder girdle of young men. Various skeletal malformations and cutaneous dermatoses have... -
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- Primary Sjogren's Syndrome Manifested asAnnular Erythema and Fever of an Unknown Origin
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Choi KW, Lee CY, Kim YH, Kim KH
- KMID: 2248076
- Korean J Dermatol.
- 2008 Oct;46(10):1391-1394.
Sjogren's syndrome is an autoimmune disorder that's characterized by dry eyes and dry mouth, and this is due to lymphocytic infiltration of the lacrimal and salivary glands. The skin lesions... -
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- Linear Macular Amyloidosis Along the Lines of Blaschko
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Ko EJ, Choi SY, Park KY, Li K, Kim BJ, Seo SJ, Kim MN, Hong CK
- KMID: 2088723
- Korean J Dermatol.
- 2013 Jul;51(7):536-538.
The primary localized cutaneous amyloidosis (PLCA) is classified into three types: macular amyloidosis, lichen amyloidosis, and nodular amyloidosis. Macular amyloidosis is characterized by pruritic, hyperpigmented macules and is most commonly... -
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- Generalized Dowling-Degos Disease: Case Reports
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Wititsuwannakul J, Noppakun N
- KMID: 2265879
- Ann Dermatol.
- 2013 Aug;25(3):360-364.
- doi: 10.5021/ad.2013.25.3.360
Dowling-Degos disease (DDD) is a rare autosomal dominant trait characterized by numerous, symmetrical, progressive and pigmented macules over the axillae, groins, face, neck, arms and trunk as well as scattered... -
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- A Case of Reticulate Pigmented Anomaly of the Flexures (Dowling-Degos Disease)
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Kang GS, Ko WT, Suh MK, Jang TJ
- KMID: 2301954
- Korean J Dermatol.
- 2009 Oct;47(10):1199-1202.
Reticulate pigmented anomaly of the flexures is a rare autosomal dominant genodermatosis, and this is also known as Dowling-Degos disease. The clinical symptoms are characterized by the progressive evolution of... -
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- Annular Erythema Associated with Anti-Ro/La Antibody Occurring in Plantar Area
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Baek YS, Kim JH, Shin WU, Kim JH, Song HJ, Oh CH
- KMID: 1440612
- Korean J Dermatol.
- 2012 Apr;50(4):350-353.
Recurrent annular erythema associated with anti-Ro/La antibody is a diagnostic term for annular erythemas that usually occurs in the face and the upper extremities of patients with positive anti-Ro/La antibodies.... -
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- A Case of Dowling-Degos Disease on the Vulva
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Kang HS, Hur J, Lee JW, Oh DH, Yeo KY, Kim JS, Yu HJ
- KMID: 2156664
- Ann Dermatol.
- 2011 May;23(2):205-208.
- doi: 10.5021/ad.2011.23.2.205
Dowling-Degos disease (DDD) is an autosomal dominant genodermatosis and this disease is a genetically determined disturbance of epidermal proliferation. It is characterized by acquired, slowly progressive pigmented lesions that primarily... -
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- Primary Cutaneous Amyloidosis with Familial Background
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Park SB, Lee Y, Seo YJ, Im M, Lee JH
- KMID: 1427472
- Korean J Dermatol.
- 2013 May;51(5):353-355.
Primary localized cutaneous amyloidosis is classified as macular, lichen, and rarely nodular amyloidosis according to clinical manifestation. Most cases are sporadic, but several cases have been reported to be familial... -
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- Neurovascular Manifestation of Loeys-Dietz Syndrome: A Case Report
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Lee YJ, Yum MS, Kim EH, Choi HW, Lee BH, Yoo HW, Ko TS
- KMID: 2055579
- J Genet Med.
- 2013 Jun;10(1):47-51.
- doi: 10.5734/JGM.2013.10.1.47
Loeys-Dietz syndrome (LDS) is an autosomal dominant disorder caused by heterozygous mutations in the genes encoding transforming growth factor-beta receptor type 1 or 2. It is typically characterized by a... -
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- Osteoma Cutis as the Presenting Feature of Albright Hereditary Osteodystrophy Associated with Pseudopseudohypoparathyroidism
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Jeong KH, Lew BL, Sim WY
- KMID: 2219385
- Ann Dermatol.
- 2009 May;21(2):154-158.
- doi: 10.5021/ad.2009.21.2.154
Primary osteoma cutis is characterized by the formation of normal bone tissue in the dermis or subcutis without any underlying tissue abnormality or pre-existing calcification. This illness is associated with... -
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- A Case of Osteoma Cutis, a Diagnostic Clue for Albright's Hereditary Osteodystrophy
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Ryu DJ, Oh SH, Han EC, Bae BG, Lee JH
- KMID: 2247921
- Korean J Dermatol.
- 2009 Apr;47(4):435-438.
Albright's hereditary osteodystrophy (AHO) has a broad spectrum of physical findings, including short stature, flattened nasal bridge, round facies, obesity, skeletal anomalies of the hands with brachydactyly, osteoma cutis, mental... -
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- Piebaldism Associated with Café-au-lait Macules and Intertriginous Freckling: A Case Report and Review of the Literature
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Akarsu S, İlknur T, Avcı C, Fetil E
- KMID: 2456236
- Ann Dermatol.
- 2019 Oct;31(5):567-570.
- doi: 10.5021/ad.2019.31.5.567
We present 9-year-old fraternal twins from a family with piebaldism, having congenital depigmented macules and meeting the diagnostic criteria for neurofibromatosis type 1 (NF1) due to the multiple café-au-lait macules... -
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- Anesthetic managements for correction of aortic valve regurgitation in a patient with Loeys-Dietz Syndrome: A case report
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Kim SH, Baek SW, Kwon WK, Kim DK, Yoon TG, Lim JA, Woo NS, Kim TY
- KMID: 2236511
- Korean J Anesthesiol.
- 2009 Sep;57(3):371-375.
- doi: 10.4097/kjae.2009.57.3.371
Loeys-Dietz Syndrome (LDS) is a recently described autosomal dominant aortic aneurysm syndrome with widespread systemic involvement. It is characterized by the triad of 1) arterial tortuosity and aneurysms, 2) hypertelorism,... -
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- A sporadic case of Loeys-Dietz syndrome type I with two novel mutations of the TGFBR2 gene
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Ha JS, Kim YH
- KMID: 2073643
- Korean J Pediatr.
- 2011 Jun;54(6):272-275.
- doi: 10.3345/kjp.2011.54.6.272
A recently recognized connective tissue disorder, Loeys-Dietz syndrome (LDS) is a genetic aortic aneurysm syndrome caused by mutations in the transforming growth factor-receptor type I or II gene (TGFBR1 or... -
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