1.The primary mediastinal liposarcoma with effusion.
Gu Tae WON ; Jin Hyun PARK ; Uk Kyun HONG ; Jae Kab LEE ; Suk Joong YONG ; Kye Chul SHIN ; So Young JIN ; Soon Hee JUNG
Tuberculosis and Respiratory Diseases 1991;38(1):65-69
No abstract available.
Liposarcoma*
2.Conglomerated Facial Liposarcoma.
Annals of Dermatology 2013;25(2):245-247
No abstract available.
Liposarcoma
3.A dedifferentiated large posterior mediastinal liposarcoma – An incidental finding successfully resected
Narasimman Sathiamurthy ; Jasjit Singh Nijhar ; Navarasi S Raja Gopal ; Premnath Nagalingam
The Medical Journal of Malaysia 2016;71(4):201-202
This is a case of a posterior mediastinal mass in an
asymptomatic gentleman, which was resected successfully
and he has been disease free for more than a year of follow
up. The histopathology findings happen to be a rare
occurrence.
Liposarcoma
4.Recurrent dedifferentiated retroperitoneal liposarcoma complicating pregnancy
Jemimah T. Cartagena‑Lim ; Kristine Therese R. Elises-Molon
Philippine Journal of Obstetrics and Gynecology 2024;48(2):117-123
Retroperitoneal liposarcoma is an uncommon tumor both in the pregnant and nonpregnant state.
Its exact incidence is unknown because of its rarity. Due to its propensity for local recurrence,
prognosis depends on histologic subtype and negative margins of resection. Surgery remains the
mainstay of treatment, and timing is critical in terms of finding a surgically resectable lesion while
balancing fetal risks. This report describes tumor recurrence in a pregnancy with a prior history of
surgery for an atypical lipomatous tumor presenting as a retroperitoneal mass. After discussion with
the multidisciplinary team, as well as with the patient’s consent, the plan was to defer surgery until
34 weeks, followed by scheduled tumor removal 2 weeks postpartum. She delivered abdominally
to a baby girl with a good outcome. Histopathology showed dedifferentiated liposarcoma with a
positive tumor margin. The patient has survived at 6-month follow-up and completed four cycles
of chemotherapy with doxorubicin, ifosfamide, and mesna. However, surveillance imaging again
showed tumor recurrence.
Liposarcoma
5.Myxoid Liposarcoma with Cartilaginous Differentiation: A Case Study with Cytogenetical Analysis.
Hyunchul KIM ; Won HWANGBO ; Sangjeong AHN ; Suhjin KIM ; Insun KIM ; Chul Hwan KIM
Korean Journal of Pathology 2013;47(3):284-288
Myxoid liposarcoma is a subtype of liposarcoma. This specific subtype can be identified based on its characteristic histological and cytogenetical features. The tumor has a fusion transcript of the CHOP and TLS genes, which is caused by t(12;16)(q13;p11). Most of the fusion transcripts that have been identified fall into three categories, specifically type I (exons 7-2), type II (exons 5-2), and type III (exons 8-2). A total of seven myxoid liposarcomas associated with the rare phenomenon of cartilaginous differentiation have been documented in the literature. Currently, only one of these cases has been cytogenetically analyzed, and the analysis indicated that it was a type II TLS-CHOP fusion transcript in both the typical myxoid liposarcoma and cartilaginous areas. This study presents a second report of myxoid liposarcoma with cartilaginous differentiation, and includes a cytogenetical analysis of both the myxoid and cartilaginous areas.
Cartilage
;
Liposarcoma
;
Liposarcoma, Myxoid
6.Myxoid Liposarcoma.
Tae Hyung KIM ; Jong Woo KIM ; Sang Won KIM ; Dong Seok KIM ; Ki Young AHN
Annals of Dermatology 1996;8(2):144-148
No abstract available.
Liposarcoma, Myxoid*
7.Liposarcoma which occured in the extremities.
Sung Joon KIM ; Tai Seung KIM ; Kwang Hyun LEE ; Jin Sub KIM ; Moon Hyang PARK ; Byoung Suck KIM
The Journal of the Korean Orthopaedic Association 1992;27(1):281-287
No abstract available.
Extremities*
;
Liposarcoma*
8.Giant Lipoma of Forearm Causing Median Nerve Compression – A Case Report
Rachana DT ; Hrishikesh PS ; Premashish JH
Journal of Surgical Academia 2016;6(2):26-29
Giant lipomas in the proximal upper extremity are rare. Traditionally these are slow growing tumour and cause
symptoms depending upon their size, position and compression of surrounding structures. Lipoma causing
compression of median nerve in the forearm is rare. Surgical excision invariably leads to complete recovery. We
present a case of a giant lipoma in forearm causing neuropathy of median nerve. It is difficult to clinically judge the
extent of lipoma in atypical position and findings. MRI should be used in pre-operative evaluation of these cases.
Surgical excision causes complete resolution of symptoms.
Lipoma
;
Liposarcoma
9.Decoded: A case report on dedifferentiated Liposarcoma on the Gluteal area
Juan Paolo David S. Villena ; Eileen Liesl A. Cubillan ; Ann Camille Q. Yuga
Acta Medica Philippina 2021;55(5):544-550
Dedifferentiated liposarcoma is a soft tissue sarcoma of adipocytic lineage. Histopathology and immunohistochemistry are essential for diagnosis. A 51-year-old Filipino woman presented with a rapidly enlarging left gluteal tumor. Histopathology revealed a multilobulated tumor having prominent myxoid stroma with numerous stellate-shaped, atypical cells bearing atypical mitotic figures. Other lobules were composed of sheets of pleomorphic cells, with atypical mitotic figures. The tumor stained positively with alcian blue, vimentin, MDM2 and p16 stains. Other immunohistochemical (IHC) studies done (pancytokeratin, CK7, CK 20, CD 34, CEA, desmin, EMA, SMA, S100) showed negative results. After a 2 cm wide excision of the sarcoma, patient was free from local tumor recurrence for 2 months, after which she was lost to follow-up. We report this case and a brief review of the current literature on dedifferentiated liposarcoma.
Liposarcoma
;
Immunohistochemistry
10.A case of myxoid liposarcoma of paratesticular tissue.
Ji Youl LEE ; Dong Hwan LEE ; Kwang Don LEE ; Young Jai LEE ; An Hi LEE
Korean Journal of Urology 1991;32(4):691-693
Liposarcoma of paratesticular origin is extremely rare and preoperative diagnosis is unusual. Myxoid type or liposarcoma is in general less malignant than testicular tumor and orchiectomy with high ligation and wide excision of tumor mass are probably the treatment of choice. We are present a case of myxoid liposarcoma and reviewed literatures.
Diagnosis
;
Ligation
;
Liposarcoma
;
Liposarcoma, Myxoid*
;
Orchiectomy