1.Effective Treatment of Suspicious Riehl's Melanosis Using Low Fluence 1,064 nm Q-switched Nd:YAG Laser and 595 nm Pulsed Dye Laser.
Sung Kyu JUNG ; Jae Beom PARK ; Byoung Joon SO ; Jie Hyun JEON ; Hwa Jung RYU ; Il Hwan KIM
Korean Journal of Dermatology 2014;52(8):589-590
No abstract available.
Lasers, Dye*
;
Melanosis*
2.Sudden Death Associated With Hypothyroidism.
Hyun Deuk CHO ; Min Kyung KIM ; Kyu Jae LEE ; Jie Hyun JEON ; Jeong Kyu LEE ; Han Kyeom KIM ; Yang Suk CHAE
Korean Journal of Legal Medicine 1999;23(2):96-100
Although it is known that hypothyroidism can cause cardiac dysfunction, it is very hard to find a case report on sudden death due to hypothyroidism. There are only two reported cases on medline; one is about a 15-year-old girl who died suddenly of Hashimoto's thyroiditis and the other is about a 31-year-old man who also died suddenly of hypothyroidism associated with chronic lymphocytic thyroiditis. Recently we found a young woman who unexpectedly died while she was sleeping. She was diagnosed as hypothyroidism when she went to hospital about a month before she died. At autopsy there were roughly four abnormal findings; Hashimoto's thyroiditis, mild chronic active hepatitis, diverticulosis and accessory spleen. Trace of chlorpheniramine was detected in gastric remains and blood alcohol level was 0.37 percent. To our knowledge, this is the first case reporting sudden and unexpected natural death associated with hypothyroidism in Korea.
Adolescent
;
Adult
;
Autopsy
;
Chlorpheniramine
;
Death, Sudden*
;
Diverticulum
;
Female
;
Hashimoto Disease
;
Hepatitis, Chronic
;
Humans
;
Hypothyroidism*
;
Korea
;
Spleen
;
Thyroid Gland
;
Thyroiditis
3.Sudden Death Associated With Hypothyroidism.
Hyun Deuk CHO ; Min Kyung KIM ; Kyu Jae LEE ; Jie Hyun JEON ; Jeong Kyu LEE ; Han Kyeom KIM ; Yang Suk CHAE
Korean Journal of Legal Medicine 1999;23(2):96-100
Although it is known that hypothyroidism can cause cardiac dysfunction, it is very hard to find a case report on sudden death due to hypothyroidism. There are only two reported cases on medline; one is about a 15-year-old girl who died suddenly of Hashimoto's thyroiditis and the other is about a 31-year-old man who also died suddenly of hypothyroidism associated with chronic lymphocytic thyroiditis. Recently we found a young woman who unexpectedly died while she was sleeping. She was diagnosed as hypothyroidism when she went to hospital about a month before she died. At autopsy there were roughly four abnormal findings; Hashimoto's thyroiditis, mild chronic active hepatitis, diverticulosis and accessory spleen. Trace of chlorpheniramine was detected in gastric remains and blood alcohol level was 0.37 percent. To our knowledge, this is the first case reporting sudden and unexpected natural death associated with hypothyroidism in Korea.
Adolescent
;
Adult
;
Autopsy
;
Chlorpheniramine
;
Death, Sudden*
;
Diverticulum
;
Female
;
Hashimoto Disease
;
Hepatitis, Chronic
;
Humans
;
Hypothyroidism*
;
Korea
;
Spleen
;
Thyroid Gland
;
Thyroiditis
4.Reconstruction of Defect on the Nasal Dorsum with Modified Bilateral Rhombic Flap.
Myeung Hoon CHOI ; Jie Hyun JEON ; Yong Ju KIM ; Kyu Chul HWANG ; Hae Jun SONG ; Chil Hwan OH ; Dong Soo YU
Korean Journal of Dermatology 2006;44(5):608-611
The skin over the nose is less mobile for primary closure of defects. In addition to skin graft and secondary intention healing, there are various local flap techniques and their modifications for the reconstruction of nasal defects. Imprecise engineering of wound repair methods and contracture can lead to twisting of the nose and distortion of surrounding anatomic structures such as the nasal ala and paranasal sulcus. The skin defects on the nasal dorsum were reconstructed with a modified bilateral rombic flap. In our case, there were no significant complications and the final result was satisfactory in both functional and cosmetic aspects. Through our experience, we can confirm that the modified bilateral rhombic flap can reconstruct defects on the center area of the nasal dorsum effectively and in a single stage.
Contracture
;
Intention
;
Nose
;
Skin
;
Transplants
;
Wounds and Injuries
5.A Case of Congenital Smooth Muscle Hamartoma Presenting as a Human Tail.
Jae Bin SHIN ; Jie Hyun JEON ; Sang Wook SON ; Hae Jun SONG ; Chil Hwan OH
Korean Journal of Dermatology 2007;45(3):287-289
A human tail is a rare congenital anomaly, and is characterised by a prominent lesion from the lumbosacrococcygeal region. Human tails are classified into 'true tails' and 'pseudotails'. True tails are comprised of only mesenchymal tissue. They are presumed to be remnants of the embryologic tail. All other lumbosacrococcygeal protrusions are summarized as pseudotails. Congenital smooth muscle hamartoma usually presents as a well-circumscribed, hypertrichotic, hyperpigmented or skin-colored patch or plaque on the trunk or an extremity at birth. Histologically, numerous thick, long, well-defined bundles of smooth muscle fibers are scattered throughout the dermis in various directions. We report a case of congenital smooth muscle hamartoma in a 15-year-old male patient who presented with a tail-like protruding mass accompanied by hypertrichosis and underlying soft tissue deviation.
Adolescent
;
Dermis
;
Extremities
;
Hamartoma*
;
Humans*
;
Hypertrichosis
;
Male
;
Muscle, Smooth*
;
Parturition
6.A Case of Recurrent Atypical Fibroxanthoma Treated with Mohs Micrographic Surgery.
Jae Bin SHIN ; Jie Hyun JEON ; Sang Wook SON ; Hae Jun SONG ; Il Hwan KIM
Korean Journal of Dermatology 2006;44(2):253-255
Atypical fibroxnathoma (AFX) is a pleomorphic spindle cell neoplasm of the dermis, and is a clinically-benign reactive lesion, despite apparently malignant histologic features. We describe a case of 16-year-old female with recurrent AFX which developed on the occipital scalp. The lesion was totally excised by Mohs micrographic surgery and no recurrence was observed during one year follow up period. It is uncommon for AFX, such as the present case, to develop on a non-sun-exposed area and in adolescence.
Adolescent
;
Dermis
;
Female
;
Follow-Up Studies
;
Humans
;
Mohs Surgery*
;
Recurrence
;
Scalp
7.A Case of Oral Focal Mucinosis.
Myeung Hun CHOI ; Jie Hyun JEON ; Aeree KIM ; Hae Jun SONG ; Chil Hwan OH
Korean Journal of Dermatology 2006;44(3):375-377
Oral focal mucinosis (OFM) is an uncommon clinicopathologic entity which is considered to be the oral counterpart of cutaneous focal mucinosis. It is comprised of a clinically-elevated mass with a histological feature of localized areas of myxomatous connective tissue. We herein report a case of oral focal mucinosis in a child, plus a review of the literature.
Child
;
Connective Tissue
;
Humans
;
Mucinoses*
8.A Case of Oral Focal Mucinosis.
Myeung Hun CHOI ; Jie Hyun JEON ; Aeree KIM ; Hae Jun SONG ; Chil Hwan OH
Korean Journal of Dermatology 2006;44(3):375-377
Oral focal mucinosis (OFM) is an uncommon clinicopathologic entity which is considered to be the oral counterpart of cutaneous focal mucinosis. It is comprised of a clinically-elevated mass with a histological feature of localized areas of myxomatous connective tissue. We herein report a case of oral focal mucinosis in a child, plus a review of the literature.
Child
;
Connective Tissue
;
Humans
;
Mucinoses*
9.A Case of Extramammary Paget's Disease Treated with 5% Imiquimod Cream.
Myeung Hun CHOI ; Jie Hyun JEON ; Sang Wook SON ; Il Hwan KIM
Korean Journal of Dermatology 2006;44(3):365-368
Extramammary Paget's disease (EMPD) is a rare intraepidermal adenocarcinoma. Mohs micrographic surgery is considered the standard treatment. Other treatment modalities such as surgical excision, radiotherapy, topical chemotherapy, and photodynamic therapy are associated with varying degrees of effectiveness, and possible loss of tissue function and disease recurrence are seen. The search for an effective, safe treatment with minimal side effects proves to be challenging. Imiquimod is the first representative of a new class of immunomodulating drugs demonstrating potent antiviral and antitumor activity, and has been approved by the FDA for treating anogenital warts, actinic keratosis and basal cell carcinoma. Recent research has demonstrated its effective usage as a 5% cream in the management of EMPD. We report a case of EMPD of the scrotum successfully treated with topical 5% imiquimod cream. This has never been published in the Korea dermatologic literature.
Adenocarcinoma
;
Carcinoma, Basal Cell
;
Drug Therapy
;
Keratosis, Actinic
;
Korea
;
Mohs Surgery
;
Paget Disease, Extramammary*
;
Photochemotherapy
;
Radiotherapy
;
Recurrence
;
Scrotum
;
Warts
10.A Case of Extramammary Paget's Disease Treated with 5% Imiquimod Cream.
Myeung Hun CHOI ; Jie Hyun JEON ; Sang Wook SON ; Il Hwan KIM
Korean Journal of Dermatology 2006;44(3):365-368
Extramammary Paget's disease (EMPD) is a rare intraepidermal adenocarcinoma. Mohs micrographic surgery is considered the standard treatment. Other treatment modalities such as surgical excision, radiotherapy, topical chemotherapy, and photodynamic therapy are associated with varying degrees of effectiveness, and possible loss of tissue function and disease recurrence are seen. The search for an effective, safe treatment with minimal side effects proves to be challenging. Imiquimod is the first representative of a new class of immunomodulating drugs demonstrating potent antiviral and antitumor activity, and has been approved by the FDA for treating anogenital warts, actinic keratosis and basal cell carcinoma. Recent research has demonstrated its effective usage as a 5% cream in the management of EMPD. We report a case of EMPD of the scrotum successfully treated with topical 5% imiquimod cream. This has never been published in the Korea dermatologic literature.
Adenocarcinoma
;
Carcinoma, Basal Cell
;
Drug Therapy
;
Keratosis, Actinic
;
Korea
;
Mohs Surgery
;
Paget Disease, Extramammary*
;
Photochemotherapy
;
Radiotherapy
;
Recurrence
;
Scrotum
;
Warts