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1.
Journal of Breast Cancer ; : 391-396, 2023.
Artículo en Inglés | WPRIM | ID: wpr-1000775

RESUMEN

Pseudoangiomatous stromal hyperplasia (PASH) is a rare idiopathic proliferative mesenchymal breast disease related to hormonal imbalance, and thus extremely rare in children and adolescents. In addition, PASH manifests as a bilateral gigantomastia in some cases with no established cause or treatment. Here, we report a case of a rapidly developed PASH presenting with bilateral gigantomastia in a 14-year-old premenarchial female patient.Considering the patient’s age and emotions and the need for nipple-areolar complex repositioning, we performed reduction mammoplasty rather than total mastectomy despite the possibility of recurrence. Although some masses could not be completely removed, no complications, such as infection, wound dehiscence, or hematoma occurred postoperatively.The patient was stable during the 18-month follow-up period, although an evidence of recurrent and residual disease was noted upon ultrasonography.

2.
Archives of Craniofacial Surgery ; : 59-61, 2017.
Artículo en Inglés | WPRIM | ID: wpr-199172

RESUMEN

As the number of people who have undergone augmentation rhinoplasty has increased recently, nasal fractures are becoming more common after rhinoplasty. A silicone implant can affect the nasal fracture pattern, but there is no significant difference in treatment methods commonly. A 28-year-old female who had undergone augmentation visited our clinic with a nasal fracture. Computed tomography revealed that the silicone implant was sandwiched between the intact nasal bones with fractured bone fragments. In this case, open reduction was inevitable and a new silicone implant was inserted after reduction. Migration of the silicone implant beneath the nasal bone is a very rare phenomenon, but its accurate prevention and diagnosis is important because a closed reduction is impossible.


Asunto(s)
Adulto , Femenino , Humanos , Diagnóstico , Hueso Nasal , Rinoplastia , Silicio , Siliconas
3.
Archives of Plastic Surgery ; : 439-443, 2017.
Artículo en Inglés | WPRIM | ID: wpr-142221

RESUMEN

Kimura disease is a rare idiopathic chronic inflammatory disorder. It typically presents in the head and neck area, whereas bilateral involvement is unusual. Its diagnosis requires it to be differentiated from other inflammatory diseases and from head and neck tumors. Treatment methods include conservative management, steroid administration, radiotherapy, and surgery; however, no single treatment of choice has been established. Herein, we report an unusual presentation of Kimura disease with bilateral parotid involvement. This case was treated by surgical excision.


Asunto(s)
Hiperplasia Angiolinfoide con Eosinofilia , Diagnóstico , Cabeza , Neoplasias de Cabeza y Cuello , Cuello , Neoplasias de la Parótida , Radioterapia
4.
Archives of Plastic Surgery ; : 439-443, 2017.
Artículo en Inglés | WPRIM | ID: wpr-142220

RESUMEN

Kimura disease is a rare idiopathic chronic inflammatory disorder. It typically presents in the head and neck area, whereas bilateral involvement is unusual. Its diagnosis requires it to be differentiated from other inflammatory diseases and from head and neck tumors. Treatment methods include conservative management, steroid administration, radiotherapy, and surgery; however, no single treatment of choice has been established. Herein, we report an unusual presentation of Kimura disease with bilateral parotid involvement. This case was treated by surgical excision.


Asunto(s)
Hiperplasia Angiolinfoide con Eosinofilia , Diagnóstico , Cabeza , Neoplasias de Cabeza y Cuello , Cuello , Neoplasias de la Parótida , Radioterapia
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