1.A Case of Progressive Cribriform and Zosteriform Hyperpigmentation.
Korean Journal of Dermatology 2013;51(4):291-295
Progressive cribriform and zosteriform hyperpigmentation (PCZH) is a distinctive syndrome first described by Rower et al. in 1978. It characteristically presents as a single area of uniformly tan, cribriform macular pigmentation with zosteriform distribution. Further, it can histologically be characterized by increased melanin pigmentation in the basal cell layer with a complete absence of nevus cells, and a lack of a preceding history of skin rash, injury or inflammation or other associated cutaneous or internal abnormalities. We herein report a case of PCZH that had developed along the right abdomen, right flank area and right back area in a 26-year-old male. The histologic investigation revealed increased melanin pigmentation in the basal layer and a distinct lack of nevus cells.
Abdomen
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Exanthema
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Humans
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Hyperpigmentation
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Inflammation
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Male
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Melanins
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Nevus
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Pigmentation
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Triacetoneamine-N-Oxyl
2.Clinical Review of Surgical Geriatric Patients over 65 Years of Age.
Hyoung Sub OH ; Joon Kil HAN ; Kwang Chan LEE
Journal of the Korean Surgical Society 1998;54(1):129-135
In order to identify the relationship between the patient's age and the presence of another disease, and the postoperative complications and mortality, we reviewed the medical records of 6156 patients admitted to the Department of Surgery, Dae Jeon Eul Ji General Hospital, during the period from January 1991 through December 1995. There were 1546 geriatric patients(>65 years of age) and 4610 adult patients (age between 16 and 64). Six hundred sixty-five patients (43%) in the geriatric group had one or more concurrent diseases preoperatively, whereas 1127 patients (24.4%) in adult group did. Postoperative complications were more frequent in the geriatric group: 21.6% (310 patients) in the geriatric group vs 15.2%(217 patients) in the adult group. Geriatric patients who had more than one concurrent disease and who underwent an emergency operation showed a higher postoperative complication rate than those who had only one concurrent disease and who underwent elective surgery. The postoperative mortality was also higher in the geriatric group: 3.8%(48 patients) in the geriatric group vs 0.7% (32 patients) in the adult group. The most frequent cause of postoperative death in the geriatric group was sepsis. The geriatric patients who had a concurrent disease account for 16.4% of postoperative complications and 1.5% of the mortalities, whereas those who did not have any concurrent disease account for 2.67% and 0.2%, respectively. Among 1127 adult patients who had a concurrent disease, 124 (11.0%) had postoperative complications and 24 (2.2%) died postoperatively. In conclusion, the elderly patients more frequently had one or more concurrent diseases, and these patients had higher postoperative complication and mortality rates, especially after emergency operations. Accordingly, it is crucial for the surgeon to completely evaluate and manage any concurrent diseases in elderly patients preoperatively.
Adult
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Aged
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Daejeon
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Emergencies
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Hospitals, General
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Humans
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Medical Records
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Mortality
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Postoperative Complications
;
Sepsis
3.Phytophotodermatitis.
Chun Bong LEE ; Eul Nam HAN ; Nack In KIM ; Choong Rim HAW
Korean Journal of Dermatology 1986;24(2):278-282
We describe herein a 3 family members with phytophotodermatitis. After fig (juice) was applied to skin for the purpose of treating psoriasis in a 30 year-old woman and applied incidentally in her mother and 3 year-old daughter, vesicobullous eruptions developed immediately after sun-exposure, predominantly in the sun-exposed area. ln histopathology, the epidermis shows intraepidermal separation with necrosis and reepithelization on basal layer and marked spongiosis. We treated with systemic steroid, wet dressing with burow solution etc, so she healed without sequela after 2 weeks.
Adult
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Bandages
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Child, Preschool
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Epidermis
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Female
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Ficusin
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Humans
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Mothers
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Necrosis
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Nuclear Family
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Psoriasis
;
Skin
4.A Case of Lymphomatoid Granulomatosis.
Ki Ho LEE ; Eul Nam HAN ; Nack In KIM ; Choong Rim HAW
Korean Journal of Dermatology 1984;22(6):684-688
We report a case of Lymphomatoid granulomatosis in a 54-year-old woman. She presented with a two months history of a tender nodule located on the left for earm associated with fever and pulmonary symptoma aggravated against various treatments. She died 92 days of admission because of respiratory failure. Diagnosis was based on the clinical features and histopathologic findings of the skin lesion.
Diagnosis
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Female
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Fever
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Humans
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Lymphomatoid Granulomatosis*
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Middle Aged
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Respiratory Insufficiency
;
Skin
5.Pedunculated Lipofibroma.
Sung Nam CHANG ; Kyeong Han YOON ; Dong Kun KIM ; Hae Eul LEE
Annals of Dermatology 1996;8(3):237-239
A 45-year-old woman had a bean-sized, asymptomatic, soft nodule on the right buttock for 4 years. Histopafhologic evaluation revealed acanthosis and a central core of adipose tissue with thin papillary and reticular dermis containing eccrine glands. Staining with alcian blue showed a slight increase of mucopolysaccharides in the reticular dermis. We made the diagnosis of pedunculated lipofibroma as a solitary form of nevus lipomatosus superficialis.
Adipose Tissue
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Alcian Blue
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Buttocks
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Dermis
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Diagnosis
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Eccrine Glands
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Female
;
Glycosaminoglycans
;
Humans
;
Middle Aged
;
Nevus
6.THE APPROACH OF SKULL BASE LESIONS IN THE VIEW POINT OF PLASTIC SURGERY.
Myung Jong LEE ; Dong Hyun KIM ; Eul Je CHO ; Suk Choo CHANG ; Han Kyu KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1997;24(3):559-569
Skull base surgery has developed through the evolution of imaging, anatomic research, surgical approach and reconstructive techniques. The basic disciplines of approaching skull base lesions are provide direct vision, minimizing brain retraction, excellent exposure and minimal blood loss. The focus of this report is to review the advantages of skull base approach in our cases and suggest some indications. We experienced 20 cases of skull base surgery by a team approach consisting of a neurosurgeon and plastic surgeon. The surgical approach were supraorbital osteotomy(5 case), orbitozygomatic osteotomy(8 case), orbitozygomaticoglenoid osteotomy (5 case ) and orbitozygomaticoglenoidocondylar osteotomy (2 case). In our experience, these approaches provided excellent exposure of the lesion, direct access to lesions and minimal brain retraction thereby better outcome.
Brain
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Osteotomy
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Skull Base*
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Skull*
;
Surgery, Plastic*
7.A Case of Benign Cephalic Histiocytosis.
Duck Hyun KIM ; Dong Sik BANG ; Shin Won HAN ; Kyoo Cheon WHANG ; Hae Eul LEE
Korean Journal of Dermatology 1986;24(3):433-438
A 18-month-old girl was seen because of an yellowish brown papular eruptions on the face, earlobes and neck of one year duration. A skin biopsy specimen revealed circumscribed cellular infiltrates composed of predorninantly pleornorphic histiocytes. Electron microscopy of biopsy material disclosed numerous worm like particles and coated vescles in limited area of the cell cytoplasm, consistent with the findinga described in benign cephalic histiocytosis. After six months of her first visit, the individual papules became flattened.
Biopsy
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Coated Vesicles
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Cytoplasm
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Female
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Histiocytes
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Histiocytosis*
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Humans
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Infant
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Microscopy, Electron
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Neck
;
Skin
8.A Case of Primary Cutaneous Plasmacytoma , Observed for 10 years.
Kyung Sool KWON ; Eul Hee HAN ; Tae Ahn CHUNG ; Suk Joo CHOI ; Joon Ho LEE
Korean Journal of Dermatology 1994;32(1):144-148
A 28-year-old female devei,oped five rice-sized erythematous telaniectatic solid papules of her left side of cheek and numerous light brownish flat papules of her face two years before visiting our department of dermatology. Biopsy results of the erythematous papule vere dermal infiltration by well-differentiated, however, somewhat atypical and varying sized plasma cells involving epidermis, and the flat papule was that of verwca plana. Bone marrow aspirate was essentially normal. Primary cutaneous plasmacytoma is a rare disease. A significant proportion of patients with this ent on to develop systemic disease with a poor prognosis. Our patient was not treatead, bit only excised partially for biopsy. All skin lesions involuted two years later spontaneously and rema ns well until now six years later without recurring.
Adult
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Biopsy
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Bone Marrow
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Cheek
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Dermatology
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Epidermis
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Female
;
Humans
;
Plasma Cells
;
Plasmacytoma*
;
Prognosis
;
Rare Diseases
;
Skin
9.A Case of Benign Cytophagic Histiocytic Panniculitis.
Joon Ho LEE ; Eul Hee HAN ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1994;32(1):99-104
Cytophagic histiocytic panniculitis is a histiocytic disorder which is characterized by recurrent subcutaneous nodules, fever, pancytopenia, and abnormal hepatocyte function. Most patients had systemic involvement with hepatosplenomegaly and pancytopenia and, after a chronic course, usually developed a hemorrhagic diathesis that led to death. Rarely reported cases were shown to have had a non-fatal course. We report herein a case of cytophagic histiocytic panniculitis in the trunk and both upper arms of 34-year-old woman who had a benign course and also showed histopatholoigcally lipomembranous change in the subcutaneous lesion.
Adult
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Arm
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Female
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Fever
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Hemorrhagic Disorders
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Hepatocytes
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Humans
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Pancytopenia
;
Panniculitis*
10.A Case of Epidermodysplasia Verruciformis Associated with Bowen's Disease.
Dae Kwang HONG ; Choon Bong LEE ; Eul Nam HAN ; Choong Rim HAW
Korean Journal of Dermatology 1986;24(2):304-309
We present a case of epidermodysplasia verruciformis a.ssociated with Bowen's disease. Patient was 33 year-old male and his skin lesions showed diffuse flat papules on face and neck, many brownish papules on trunk and papillomatous tumors also appeared un scalp and post auricular area, Skin biopsy findings from the flat papular lesion showed histopathologic features of verruca plana and from the papillomatous lesion showed the feature of Bowen's disease. Electron microscopic finding from the flat papular lesion showed marked aggregates of viral particles around the nuclei of epidermal keratinocytes.
Adult
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Biopsy
;
Bowen's Disease*
;
Epidermodysplasia Verruciformis*
;
Humans
;
Keratinocytes
;
Male
;
Neck
;
Scalp
;
Skin
;
United Nations
;
Virion
;
Warts