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1.
Archives of Reconstructive Microsurgery ; : 56-59, 2016.
Article in English | WPRIM | ID: wpr-159399

ABSTRACT

Eccrine porocarcinoma is a rare malignant neoplasm of the eccrine sweat gland that often occurs in the lower extremities, and usually affects elderly individuals. Most cases of eccrine porocarcinoma arise de novo. We encountered a case of a large porocarcinoma arising in a pre-existing ganglion cyst in the knee. The malignant tumor was excised widely, and the defect was reconstructed using a free anterolateral thigh flap.


Subject(s)
Aged , Humans , Eccrine Porocarcinoma , Ganglion Cysts , Knee , Lower Extremity , Sweat Glands , Thigh
2.
Archives of Aesthetic Plastic Surgery ; : 149-152, 2016.
Article in English | WPRIM | ID: wpr-93266

ABSTRACT

We present our experience with calvarial bone framework insertion through an intraoral approach for a patient who was at risk for columellar necrosis due to a previous open rhinoplasty. A 58-year-old woman exhibited severe columellar contracture, so that the columellar tissue was too fragile to be touched. We could not incise the columella and insert a new nasal implant through the bilateral rim incision. Moreover, the patient had septal cartilage perforation and collapse. The patient needed columellar support as well as nasal dorsum reconstruction. The authors decided to graft an autogenous L-strut bone framework through an intraoral approach. Two pieces of 5-cm × 1-cm sized split calvarial bone were harvested and trimmed to fit the width and length of the nasal dorsum and columella. The right-angle-shaped bone framework was made with an absorbable plate and screws. Through a gingivobuccal incision, the bone framework graft was inserted and the graft was fixed with absorbable screws. The patient did not experience complications such as skin necrosis or inflammation. A bone framework grafted through an intraoral approach can be a good choice for patients who have experienced scar contracture in the columella, septal cartilage perforation, and collapse.


Subject(s)
Female , Humans , Middle Aged , Cartilage , Cicatrix , Contracture , Inflammation , Necrosis , Oral Surgical Procedures , Rhinoplasty , Skin , Transplants
3.
Archives of Craniofacial Surgery ; : 218-221, 2016.
Article in English | WPRIM | ID: wpr-89537

ABSTRACT

Temporal hollowing is a common complication that occurs after coronal approach surgeries. However, temporal hollowing without previous nerve damage or trauma history is rare. Herein, we present a patient with cryptogenic temporal hollowing. A 22-year-old man without any history of craniofacial interventions or trauma presented with temporal hallowing. Magnetic resonance imaging revealed fatty degeneration of the left temporalis muscle. Electromyography and nerve conduction study showed no signs of neurologic abnormalities. The patient received autologous fat injection of 30 mL harvested from the left thigh using the modified Coleman technique. Temporal hollowing is commonly caused by atrophy of the superficial temporal fat pad. Its incidence is reported to be as high as 6% after coronal approach operation. Augmentation using porous hydroxyapatite or titanium mesh is a treatment option. Autologous fat graft can also be an option for mild to moderate temporal hollowing. In this case, a patient with no history of trauma, surgery, or myogenic disease developed temporal hollowing. Further study of the littleknown cryptogenic form of temporal hollowing is warranted.


Subject(s)
Humans , Young Adult , Adipose Tissue , Atrophy , Durapatite , Electromyography , Incidence , Magnetic Resonance Imaging , Neural Conduction , Thigh , Titanium , Transplants
4.
Archives of Plastic Surgery ; : 582-585, 2016.
Article in English | WPRIM | ID: wpr-113635

ABSTRACT

It is uncommon for a palatal fistula to be detected in individuals who have not undergone surgery, and only sporadic cases have been reported. It is even more difficult to find cases of acquired palatal fistula in patients with submucous or incomplete cleft palate. Herein, we present 2 rare cases of this phenomenon. Case 1 was a patient with submucous cleft palate who acquired a palatal fistula after suffering from oral candidiasis at the age of 5 months. Case 2 was a patient with incomplete cleft palate who spontaneously, without trauma or infection, presented with a palatal fistula at the age of 9 months.


Subject(s)
Humans , Candidiasis, Oral , Cleft Palate , Fistula , Oral Fistula
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