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1.
Korean Journal of Dermatology ; : 472-475, 2020.
Article | WPRIM | ID: wpr-832630

ABSTRACT

Fibrofolliculoma is a benign perifollicular connective tissue tumor that usually occurs in the face. Most fibrofolliculoma present as multiple lesions and typically occur with trichodiscomas and acrochordons, constituting the Birt-Hogg-Dube syndrome. Solitary fibrofolliculoma is nonhereditary and unassociated with other cutaneous abnormalities. A 72-year-old man visited our clinic complaining of a solitary umbilicated nodule on the antitragus of the left ear. Skin biopsy from the lesion showed a central dilated follicular infundibulum with anastomosing bands of follicular epithelium extending into the fibrous stroma. The diagnosis of a solitary fibrofolliculoma was made based on the clinical and histopathological findings. No signs of lesion recurrence for 1 year after shave removal were noted. We report a rare case of solitary fibrofolliculoma that occurred on the antitragus of the ear.

2.
Annals of Dermatology ; : 595-600, 2019.
Article in English | WPRIM | ID: wpr-762398

ABSTRACT

BACKGROUND: Chronic hand eczema (CHE) tends to be refractory to conventional therapy. Previous clinical trials have found that alitretinoin is an effective and well-tolerated treatment for CHE. However, there is a relative lack of data on the effectiveness of alitretinoin in elderly patients. OBJECTIVE: The aim of this study was to investigate the efficacy and safety of oral alitretinoin in elderly patients with moderate to severe CHE in Korea. METHODS: We retrospectively investigated 46 CHE patients who were treated with either 10 mg or 30 mg of alitretinoin between June of 2016 and July of 2018. The physician's global assessment (PGA) was used to evaluate treatment efficacy. All adverse events were retrospectively evaluated with respect to laboratory testing, including complete blood cell count, fasting blood chemistry, lipid profile, and liver and thyroid function tests. RESULTS: The mean patient age in this study was 71.0±5.1 years. The treatment period was over eight weeks. A total of 38 of 46 patients (82.6%) exhibited clinical improvement with PGA ratings of ‘clear’ or ‘almost clear.’ There were 13 patients (28.3%) who experienced an adverse effect, with the most common being headache (13.0%) and gastrointestinal symptoms (8.7%) followed by xerosis (6.5%). A total of 13 patients developed or exhibited worsening hypertriglyceridemia (28.3%). CONCLUSION: Alitretinoin can be considered a safe and effective treatment option in elderly patients with moderate to severe CHE.


Subject(s)
Aged , Humans , Blood Cell Count , Chemistry , Eczema , Fasting , Hand , Headache , Hypertriglyceridemia , Korea , Liver , Retrospective Studies , Thyroid Function Tests , Treatment Outcome
3.
Korean Journal of Dermatology ; : 551-555, 2019.
Article in English | WPRIM | ID: wpr-786276

ABSTRACT

Nivolumab is a fully-humanized IgG4 monoclonal antibody that competitively binds to the programmed cell death receptor-1 protein (an immune check-point molecule) present on activated T cells. Nivolumab is approved for the treatment of advanced melanoma, lung cancer, and renal cell carcinoma. It attenuates the inactivation of cytotoxic CD8+ T cells and, produces an antitumor effect; however it may be associated with immune-related adverse events, including the development of lichen planus (LP). A 72-year-old man presented with a 2-month history of multiple, polygonal, purplish papules on the dorsal aspect of both hands. He was diagnosed with large cell neuroendocrine carcinoma (LCNEC) of the lung 4 years earlier and was treated with nivolumab (3 mg/kg every 2 weeks) for 9 months. By the 14th course of nivolumab therapy, the patient developed multiple rashes on the dorsal aspect of both hands, and biopsy was consistent with findings of LP. We report a rare case of LP in a patient with lung cancer treated with nivolumab.


Subject(s)
Aged , Humans , Biopsy , Carcinoma, Neuroendocrine , Carcinoma, Renal Cell , Cell Death , Exanthema , Hand , Immunoglobulin G , Lichen Planus , Lichens , Lung Neoplasms , Lung , Melanoma , T-Lymphocytes
4.
Annals of Dermatology ; : 704-707, 2018.
Article in English | WPRIM | ID: wpr-718551

ABSTRACT

Parry Romberg Syndrome (PRS), also known as idiopathic progressive hemifacial atrophy, is a rare neurocutaneous disorder characterized by loss of skin and subcutaneous fat of face, muscles, and bones causing unilateral atrophy. Most patients require only soft tissue augmentation although syndrome has varying grades of severity. In the majority of reported cases, it has been treated with surgical flap or autologous fat transplantation. However, these treatments need complicated surgical skills which take a lot of time and cost. Herein we report the first case of PRS augmented by hyaluronic acid (HA) filler in a 42-year-old female patient to suggest that HA filler could be a safe, simple, and even rational economic alternative to surgical treatment.


Subject(s)
Adult , Female , Humans , Atrophy , Facial Hemiatrophy , Hyaluronic Acid , Muscles , Neurocutaneous Syndromes , Skin , Subcutaneous Fat , Surgical Flaps
5.
Korean Journal of Dermatology ; : 485-488, 2018.
Article in Korean | WPRIM | ID: wpr-717029

ABSTRACT

Lichen sclerosus et atrophicus (LSA) is a chronic inflammatory dermatosis presenting as white papules and atrophic patches in the anogenital region. Extragenital LSA is rare and commonly affects the neck, thighs, and the trunk. A 68-year-old woman presented with a well-demarcated, whitish linear plaque on the forehead that was observed several months prior to presentation. A biopsy specimen showed hyperkeratosis and thinning of the epidermis and homogenization of collagen in the papillary dermis with a subepidermal cleft. Mild periappendageal lymphocytic infiltration and eccrine gland atrophy secondary to thickening of collagen bundles were observed in the deep dermis. Based on the clinical and histopathological findings, this patient was diagnosed with extragenital LSA and concomitant morphea along the Blaschko's lines.


Subject(s)
Aged , Female , Humans , Atrophy , Biopsy , Collagen , Dermis , Eccrine Glands , Epidermis , Forehead , Lichen Sclerosus et Atrophicus , Lichens , Neck , Scleroderma, Localized , Skin Diseases , Thigh
6.
Korean Journal of Dermatology ; : 344-345, 2018.
Article in Korean | WPRIM | ID: wpr-714946

ABSTRACT

No abstract available.


Subject(s)
Carcinoma, Basal Cell
7.
Annals of Dermatology ; : 483-486, 2017.
Article in English | WPRIM | ID: wpr-86509

ABSTRACT

Multiple myeloma (MM) can be defined as a malignancy with monoclonal plasma cell proliferation. A 66-year-old man presented with pruritic erythematous to purplish plaque grouped nodule with black pigmentations and purpura on the right forearm. The patient was diagnosed with MM about five years prior to the visit at our hospital. Erythematous plaque on his right arm grew rapidly in size over one month and appeared about seven months after the fracture surgery. Skin biopsy showed multiple plasma cell infiltration with monoclonality for lambda light chain, which was consistent with cutaneous plasmacytoma. The patient refused to be treated and died two months later. We herein report an interesting case of cutaneous plasmacytoma at the surgical site of fracture repair.


Subject(s)
Aged , Humans , Arm , Biopsy , Forearm , Multiple Myeloma , Neoplasm Metastasis , Pigmentation , Plasma Cells , Plasmacytoma , Purpura , Skin
8.
Annals of Dermatology ; : 334-336, 2017.
Article in English | WPRIM | ID: wpr-93892

ABSTRACT

Eccrine squamous syringometaplasia (ESS) is a histologically distinctive skin eruption occurring predominantly in acral or intertriginous areas presenting as erythematous macules, papules or patches. The etiology of ESS remains unclear, but it is usually reported in patients receiving chemotherapy for various malignant neoplasms. To date, only two cases of ESS associated with non-steroidal anti-inflammatory drugs (NSAIDs), which has distinctive clinical features and pathogenesis, have been reported in the literature. Herein, we report a rare and interesting case of ESS associated with pelubiprofen, a recently developed NSAID, which appeared after pelubiprofen therapy and resolved spontaneously after discontinuing the medication.


Subject(s)
Humans , Dermatitis, Phototoxic , Drug Therapy , Metaplasia , Skin
9.
Annals of Dermatology ; : 749-752, 2016.
Article in English | WPRIM | ID: wpr-25360

ABSTRACT

Kaposi's sarcoma is a multifocal proliferative vascular tumor involving the skin and other organ and psoriasis is a chronic cutaneous disease with papules and plaques with white scale. Development of Kaposi's sarcoma in psoriasis patients has been reported rarely. A 71-year-old man presented with multiple brownish to violaceous plaques on both feet and arms which were found 4 months ago. The biopsy confirmed Kaposi's sarcoma. The patient was diagnosed with psoriasis vulgaris 10 years ago and Kaposi's sarcoma lesions developed between psoriatic plaques. We herein report a rare case of simultaneous occurrence of Kaposi's sarcoma and psoriasis vulgaris which need quite different treatment.


Subject(s)
Aged , Humans , Arm , Biopsy , Foot , Psoriasis , Sarcoma, Kaposi , Skin
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