🐕 Lee Soo Hyuk Plastic Surgery

LeeSoo Hyuk PROFILE Lee Soo Hyuk (born - 이혁수 Lee Hyuk Soo) Model, Actor DOB: 1988.5.31 Hometown: Gwacheon, Gyeonggi Province Height - 6'1"~6'2" Instagram: leesoohyuk FILMOGRAPHY TV White Christmas (KBS2 2011) Deep Rooted Tree (SBS 2011) What's Up (MBN 2011) Vampire Idol (MBN 2011) Shark (KBS2 20 Overview Locations Reviews Photos Q&A Videos Procedures I'm known for Total years in practice 8 Dr. James Lee is dedicated to enhancing appearance and self-image by providing the most comfortable, compassionate, and meticulous care possible. His attention to detail and artistic vision ensure that every procedure is specifically tailored for each patient. Consultation Fee $200. Get a consultation Now you can select a doctor with confidence. Verified doctors complete our multistep verification process, fulfill all requirements for every treatment offered, commit to extraordinary patient communication, and meet a higher standard. Now you can select a doctor with confidence. Verified doctors complete our multistep verification process, fulfill all requirements for every treatment offered, commit to extraordinary patient communication, and meet a higher standard. License reviewed within last 3 months Minimum 4 out of 5 star patient rating Responds within 2 business days Locations Explore video content uploaded by Dr. Lee LeeSoo Hyuk memulai debutnya di dunia modeling pada 2006 dalam sebuah peragaan busana untuk koleksi desainer Jung Wook Jun. Setelah penampilannya dalam acara tersebut Soo Hyuk tampil sebagai model di beberapa cover majalah gaya hidup ternama seperti GQ, Bazaar dan Elle. Lee Soo Hyuk Foto: Dok. tvN, Instagram @leesoohyuk, SSTV Journal List Medicine Baltimore 2022 Nov 4 PMC9646658 Medicine Baltimore. 2022 Nov 4; 10144 e31360. Jun Ho Choi, MD,a Soo Hyuk Lee, MD,a Kwang Seog Kim, MD, PhD,a,* Yoo Duk Choi, MD, PhD,b Jae Ha Hwang, MD, PhD,a and Sam Yong Lee, MD, PhDaRationaleMyxoid pleomorphic liposarcoma MPL is a rare aggressive adipocytic tumor that mainly presents in children and adolescents. It is most frequently observed in the mediastinum and rarely in the head and neck, perineal region, or back. Herein, we report the first published case of MPL of the teres minor concernsA 24-years-old woman presented with a painless palpable mass in her right resonance imaging identified a × × cm mass suspected to be a sarcoma in the teres minor muscle. Positron emission tomography/computed tomography revealed no evidence of distant metastasis. Histopathological examination revealed the mass to be an MPL, which was assigned a histologic grade of 3 according to the French Federation of Cancer Centers Sarcoma Group system. No tumor cells were observed along the resected general anesthesia, the right teres minor muscle containing the mass was excised en bloc and frozen biopsy confirmed that the tumor cells did not invade the surrounding patient underwent radiotherapy and was followed up for 6 months without MPL in the teres minor muscle is rare, it should be considered in the differential diagnosis in patients with a mass in the teres minor muscle due to its poor liposarcoma, Myxoid, pleomorphic, rotator cuff, teres minor1. IntroductionFirst described by Alaggio et al[1] in 2009, myxoid pleomorphic liposarcoma MPL is an extremely rare, aggressive adipocytic tumor with a high risk of metastasis and recurrence. MPL has been considered a separate entity in the World Health Organization classification of soft tissue tumors since 2020.[2] MPL has mixed histological characteristics with conventional myxoid and pleomorphic liposarcomas.[2] Genetically, MPL lacks damage-inducible transcript 3 DIT3 rearrangement and recurrent mouse double minute 2 homolog mouse double minutes 2 homolog MDM2 amplification.[2]MPL occurs predominantly in female children and adolescents.[2] It is observed most frequently in the mediastinum and rarely in the head and neck, perineal region, or back.[2] However, there have been no reports of MPL in the teres minor muscles. Herein, we report the first published case of MPL of the teres minor Case presentationA 24-years-old woman presented with a painless palpable mass in her right shoulder. The mass was detected 4 months prior and grew rapidly Fig. 1. Shoulder magnetic resonance imaging showed a × × cm mass resembling sarcoma in the right teres minor muscle Fig. 2. Positron emission tomography/computed tomography showed no evidence of distant photograph of a 24-years-old woman with a mass on her right posterior resonance imaging showing a × × cm heterogeneous soft tissue mass with a myxoid component in the teres minor muscle. A Contrast-enhanced T1-weighted imaging. B Fat-suppressed T2-weighted patient had a history of treatment for other tumors twice during childhood. The first tumor was a teratoma in her right ovary at 2 years of age; the second was a rhabdomyosarcoma in her right nostril at 3 years of age. Consequently, the mass in her teres minor muscle was suspected to be a malignant tumor associated with a germline mutation. However, no other family member had a history of cancer, and the test for germline mutations in the TP53 tumor suppressor gene, which are mainly found in Li-Fraumeni syndrome LFS, was also general anesthesia, the entire area of the right teres minor muscle, including the mass, was excised en bloc, and frozen biopsy confirmed that the tumor cells had not invaded the surrounding tissues Fig. 3. Histopathological examination revealed the mass to be MPL Fig. 4. The histologic grade was 3 according to the French Federation of Cancer Centers Sarcoma Group system. No tumor cells were observed along the resected margins. Four cycles of radiotherapy were performed. No recurrence or metastasis was observed for 6 months; however, further workup was not possible as the patient refused evaluation of possible associated malignant tumors and genetic photographs. A Operating field after en bloc excision of the mass with the surrounding right teres minor muscle. B Cross-section of the mass showing yellow adipose-like appearance in the periphery and myxoid changes in the examination revealing the mass to be myxoid pleomorphic liposarcoma. Photomicrographs showing A lymphangioma-like myxoid pools within the tumor H&E, ×40; B spindle to ovoid primitive tumor cells, lipoblasts, and a delicate curvilinear capillary vasculature H&E, ×100; and C scattered pleomorphic cells and pseudocystic changes H&E, ×100. H&E = hematoxylin and eosin DiscussionLiposarcomas are divided into three histological subtypes well- and de-differentiated liposarcoma, myxoid/round cell liposarcoma, and pleomorphic liposarcoma.[3] Each subtype is characterized by specific genetic changes that are presumed to induce tumor initiation.[3] MPL is a subtype of liposarcoma recently defined by Alaggio et al[1] in 2009 that shows mixed histological characteristics of conventional myxoid liposarcoma and pleomorphic liposarcoma.[4] MPL shows no fused in sarcoma/Ewing’s sarcoma RNA binding protein 1 ESWR1-damage-inducible transcript 3 fusions, as observed in myxoid liposarcoma, and there is no amplification associated with the MDM2 nuclear gene, as observed in well-differentiated or de-differentiated liposarcoma.[2] In the present case, histopathological biopsy showed a mixture of lymphangioma-like myxoid pools and scattered pleomorphic cells with pseudocystic changes Fig. 4. Our patient showed weak immunoreactivity for S100, Ki-67, and integrase interactor 1. Cluster of differentiation CD68, CD34, and MDM2 were MPLs are large and typically occur in young women.[2] MPL occurs in the mediastinum, head and neck, extremities, abdominal cavity, and trunk.[5] MPL is associated with high local recurrence, distant metastasis, and low survival rates.[6] Furthermore, age ≥ 60 years, non-extremity lesions, deep tumors, and large tumors diameter ≥ 5 cm are associated with poor prognosis.[6] However, there are no agreed-upon recommendations in the management standards associated with MPL.[5] In our case, the MPL measured × × cm and was located on the shoulder of a 24-years-old woman. Similar to the surgical treatment of liposarcoma, the tumor was removed en bloc with the surrounding teres minor muscle, with no tumor cells observed in the resected margin. Although frozen biopsy confirmed that the tumor cells did not invade the surrounding tissues, radiotherapy was performed to prevent local metastasis. No recurrence or metastasis was observed for 6 tissue tumors are overwhelmingly benign, with lipomas predominating.[7] Lipomas are the most common soft tissue tumors and occur in various regions of the body, including the shoulder.[8,9] However, while malignant tumors can occur in the shoulder, such as liposarcoma, myxofibrosarcoma, pleomorphic undifferentiated sarcoma, dermatofibrosarcoma protuberans, synovial sarcoma, leiomyosarcoma, and malignant peripheral nerve sheath tumors,[7] malignant tumors in the teres minor muscles are rare. A literature search of the Ovid, PubMed, Scopus, and Web of Science electronic databases on June 30, 2022, using the terms teres minor, sarcoma, carcinoma, cancer, malignant tumor, and malignancy and without date or language restriction, revealed no other rotator cuff is a muscle group composing the supraspinatus, infraspinatus, subscapularis, and teres minor. This muscle group stabilizes the shoulder joint and centers the humeral head in the glenoid cavity. Although the teres minor muscle primarily provides external rotation of the shoulder joint, the infraspinatus muscle is the main external rotator of the shoulder joint. Therefore, if the infraspinatus muscle is healthy, the absence of the teres minor muscle has little effect on shoulder joint function.[10] Following the en bloc resection of the MPL surrounded by the teres minor muscle, the patient did not complain of shoulder function discomfort and did not request further evaluation or case reports have described an association between MPL and LFS in adolescents and young adults.[11–13] The characteristic tumors in the LFS spectrum include soft tissue sarcomas, osteosarcomas, brain tumors, premenopausal breast cancers, adrenal cortical carcinomas, and leukemias.[14] The patient in the present case had a history of teratoma in the right ovary at 2 years of age, rhabdomyosarcoma in the right nostril at 3 years of age, and MPL in the teres minor muscle at 23 years of age. However, analysis of a blood sample did not show a germline mutation in TP53, and the patient’s family history did not correspond to the LFS criteria. A relationship between complex chromosomal alterations and MPL has also recently been reported.[4] While additional whole-genome sequencing tests were recommended to detect other genetic disorders, the patient is the first case report of an MPL in the teres minor muscle. Although MPL in the teres minor muscle is rare, due to its poor prognosis, this condition should be considered in the differential diagnosis in patients with a mass in the teres minor contributionsConceptualization Kim curation Choi JH, Lee analysis Choi YD, Hwang JH, Lee Choi YD, Hwang JH, Lee administration Kim Choi JH. Lee - original draft Choi JH, Lee SH, Kim KS, Choi YD, Hwang JH, Lee - review & editing Kim =cluster of differentiationDIT3 =damage-inducible transcript 3EWSR1 =Ewing’s sarcoma RNA binding protein 1FUS =fused in sarcomaINI1 =integrase interactor 1LFS =Li-Fraumeni syndromeMDM2 =mouse double minute 2 homologMPL =myxoid pleomorphic liposarcomaAll data generated or analyzed during this study are included in this published article [and its supplementary information files]The authors have no funding and conflicts of interest to study was approved by the Institutional Review Board of Chonnam National University Hospital IRB No., CNUH-EXP-2022-156 and conducted in accordance with the principles of the Declaration of Helsinki. Written informed consent for publication of the clinical details and images was obtained from the to cite this article Choi JH, Lee SH, Kim KS, Choi YD, Hwang JH, Lee SY. Myxoid pleomorphic liposarcoma in the teres minor muscle A case report. Medicine 2022;10144e31360.References[1] Alaggio R, Coffin CM, Weiss SW, et al.. Liposarcomas in young patients a study of 82 cases occurring in patients younger than 22 years of age. Am J Surg Pathol. 2009;33645–58. [PubMed] [Google Scholar][2] Choi JH, Ro JY. The 2020 WHO classification of tumors of soft tissue selected changes and new entities. Adv Anat Pathol. 2021;2844–58. [PubMed] [Google Scholar][3] Crago AM, Dickson MA. Liposarcoma multimodality management and future targeted therapies. Surg Oncol Clin N Am. 2026;25761–73. [PMC free article] [PubMed] [Google Scholar][4] Creytens D, Folpe AL, Koelsche C, et al.. Myxoid pleomorphic liposarcoma-a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma. Mod Pathol. 2021;342043–9. [PubMed] [Google Scholar][5] Haddox CL, Riedel RF. Recent advances in the understanding and management of liposarcoma. Fac Rev. 2021;101. [PMC free article] [PubMed] [Google Scholar][6] Gami S, Tiwari SB, Gautam K, et al.. A rare case of myxoid pleomorphic liposarcoma in an infant a report. Int J Surg Case Rep. 2021;87106365. [PMC free article] [PubMed] [Google Scholar][7] Hallinan J, Huang BK. Shoulder tumor/tumor-like lesions what to look for. Magn Reson Imaging Clin N Am. 2020;28301–16. [PubMed] [Google Scholar][8] Koh IS, Kim JW, Yun JY, et al.. Bilateral symmetrical lipoma of the buccal fat pad as an incidental finding in a woman with weight gain after tamoxifen a case report. Arch Craniofac Surg. 2021;22329–32. [PMC free article] [PubMed] [Google Scholar][9] Jang N, Shin HW, Kim J, et al.. A case report of Madelung’s disease. Arch Craniofac Surg. 2020;21305–8. [PMC free article] [PubMed] [Google Scholar][10] Williams MD, Edwards TB, Walch G. Understanding the importance of the teres minor for shoulder function functional anatomy and pathology. J Am Acad Orthop Surg. 2018;26150–61. [PubMed] [Google Scholar][11] Francom CR, Leoniak SM, Lovell MA, et al.. Head and neck pleomorphic myxoid liposarcoma in a child with Li-Fraumeni syndrome. Int J Pediatr Otorhinolaryngol. 2019;123191–4. [PubMed] [Google Scholar][12] Sinclair TJ, Thorson CM, Alvarez E, et al.. Pleomorphic myxoid liposarcoma in an adolescent with Li-Fraumeni syndrome. Pediatr Surg Int. 2017;33631–5. [PubMed] [Google Scholar][13] Zare SY, Leivo M, Fadare O. Recurrent pleomorphic myxoid liposarcoma in a patient with Li-Fraumeni syndrome. Int J Surg Pathol. 2020;28225–8. [PubMed] [Google Scholar][14] Kamihara J, Rana HQ, Garber JE. Germline TP53 mutations and the changing landscape of Li-Fraumeni syndrome. Hum Mutat. 2014;35654–62. [PubMed] [Google Scholar]Articles from Medicine are provided here courtesy of Wolters Kluwer Health DaWoon Lee currently works at the Department of Plastic Surgery, Soon Chun Hyang University Hospital. Da Woon does research in Plastic Surgery, Infectious Diseases and Dermatology.

LeeSoo-hyuk. (Actor) Lee Soo-hyuk is a South Korean model turned actor popularly known as Lee. His impeccable fashion sense has made him a fashion icon among the Korean youth. Lee has walked the ramp and has posed for numerous high profile designers and photographers. His chiseled face and well-shaped body have made him the most sought-after

^{LeeSoo-hyuk (Korean: 이수혁; born Lee Hyuk-soo on May 31, 1988) is a South Korean model and actor. (en) Lee Soo-hyuk (Hangul: 이수혁; lahir Lee Hyuk-soo; lahir 31 Mei 1988) adalah model dan aktor asal Korea Selatan. (in) イ・スヒョク（李洙赫、1988年5月31日 - ）は、韓国ソウル特別市出身のモデル、俳優。} BornLee Hyuk-soo, he debuted as a model in designer Jung Wook-jun's Lone Costume fashion show in 2006. He walked down the runways of the nation's famous fashion brands including General Idea and Song Zio, and did cover shoots for several renowned fashion magazines such as GQ, Bazaar and Elle. After appearing in music videos of girl groups Gavy . 285 404 336 209 83 456 76 112

lee soo hyuk plastic surgery