scholarly journals A case report of primary myxoid liposarcoma mimicking as a parotid cystic lesion

Medicine ◽  
2022 ◽  
Vol 101 (2) ◽  
pp. e28473
Author(s):  
Yong Tae Hong ◽  
Yunna Yang ◽  
Hyunjun Lee
Keyword(s):  
Case Report ◽  
Cystic Lesion ◽  
Myxoid Liposarcoma

scholarly journals Concomitant cemento-osseous dysplasia and aneurysmal bone cyst of the mandible: a rare case report with literature review

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Han-Gyeol Yeom ◽  
Jung-Hoon Yoon
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Aneurysmal Bone Cyst ◽  
Cystic Lesion ◽  
Bone Cyst ◽  
Neck Region ◽  
Diagnostic Process ◽  
Simultaneous Occurrence ◽  
Head And Neck Region ◽  
Osseous Dysplasia

Abstract Background Concomitant cemento-osseous dysplasia (COD) and aneurysmal bone cyst (ABC) are rare in the head and neck region. In our search of the English language literature, we found only one case report describing the simultaneous occurrence of COD and ABC in the head and neck region. Here, we report a case of COD associated with ABC. Further, we performed a systematic search of the literature to identify studies on patients with COD associated with nonepithelial lined cysts of the jaws. Case presentation The patient was a 32-year-old woman who was referred from a private dental clinic because of a cystic lesion below the mandibular right first molar. She had no pain or significant systemic disease. After performing panoramic radiography and cone-beam computed tomography, the imaging diagnosis was COD with a cystic lesion, such as ABC or solitary bone cyst. Excisional biopsy was performed, which revealed concomitant COD and ABC. Conclusion This case of ABC associated with COD provides insight for the diagnostic process of radiographically mixed lesions with cystic changes.

Recurrent retroperitoneal myxoid liposarcoma during pregnancy: a case report and literature review

2005 ◽  
Vol 15 (6) ◽  
pp. 1235-1238 ◽  
Author(s):  
C.-J. JENG ◽  
C.-Y. TZEN ◽  
W.-C. HUANG ◽  
Y.-C. YANG ◽  
J. SHEN ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Myxoid Liposarcoma

Peri-Implant Cystic Lesion With Unusual Cellular Changes: A Case Report

2014 ◽  
Vol 4 (4) ◽  
pp. 240-245 ◽  
Author(s):  
Bryan J. Frantz ◽  
Jack G. Caton ◽  
Fred J. Bonacci ◽  
Alessandro Geminiani ◽  
Remì Arseneau ◽  
...  
Keyword(s):  
Case Report ◽  
Cystic Lesion ◽  
Cellular Changes

scholarly journals Solitary pancreatic metastasis of extremity myxoid liposarcoma: a case report and literature review

BMC Cancer ◽  
2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Dingding Wang ◽  
Jie Wu ◽  
Jian Yu ◽  
Hong Zhang ◽  
Honggang Liu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Myxoid Liposarcoma ◽  
Pancreatic Metastasis

Primary meningeal myxoid liposarcoma with aggressive behavior after recurrence: case report

2018 ◽  
Vol 160 (8) ◽  
pp. 1557-1561
Author(s):  
Noriyuki Watanabe ◽  
Haruo Ohtani ◽  
Shuichi Mori ◽  
Masahiro Iguchi ◽  
Alexander Zaboronok ◽  
...  
Keyword(s):  
Case Report ◽  
Aggressive Behavior ◽  
Myxoid Liposarcoma

scholarly journals LIPOSARCOMA OF SPERMATIC CORD PRESENTING AS INDIRECT INGUINAL HERNIA- A RARE CASE REPORT

2011 ◽  
Vol 01 (01/03) ◽  
pp. 63-65
Author(s):  
Padma Shetty K. ◽  
Harish S. Permi ◽  
Michelle Mathias ◽  
Kishan Prasad ◽  
Teerthanath S. ◽  
...  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Case ◽  
Surgical Excision ◽  
Myxoid Liposarcoma ◽  
Clinical Findings ◽  
Inguinal Region ◽  
Indirect Inguinal Hernia ◽  
Rare Case Report

AbstractLiposarcoma in the inguinal region though rare are clinically significant lesions. Preoperative diagnosis is difficult since the clinical findings are very similar to that of inguinal hernia. We report a rare case of Liposarcoma of the spermatic cord in 85 year old male, clinically diagnosed as left sided indirect inguinal hernia. Surgical excision specimen showed multiple globular lipomatous masses which were yellowish and grey tan with areas of myxoid degeneration and necrosis seen. Microscopic examination showed adipocytes arranged in lobules with numerous blood vessels, lipoblasts and myxoid stroma confirming the diagnosis of myxoid liposarcoma. He is on regular follow up since two years without any recurrence or metastasis. Our case report highlights the importance of sampling and examination of fatty masses in the inguinal region to rule out the possibility of liposarcoma as they are mistaken for lipoma at surgery.

Lymphoepithelial cyst of the pancreas. A case report

2007 ◽  
Vol 52 (3) ◽  
pp. 53-53
Author(s):  
L Fraser ◽  
OO Komolafe ◽  
JR Anderson
Keyword(s):  
Case Report ◽  
Cystic Lesion ◽  
Cystic Lesions ◽  
Lymphoepithelial Cyst ◽  
Invasive Procedures ◽  
Diagnostic Challenge ◽  
Distal Pancreas ◽  
Ct And Mri ◽  
Diagnostic Investigations ◽  
The Ideal

We present the case of a 63 year-old male who presented with a cystic lesion of the distal pancreas. Excision and histology showed this to be a lymphoepithelial cyst. Cystic lesions of the pancreas represent a diagnostic challenge, especially when pseudocyst secondary to pancreatitis is excluded. These lesions can be broadly classified into benign, pre-malignant and malignant. Widely used imaging modalities such as CT and MRI are not able to categorically differentiate between these. More invasive procedures such as endoscopic US and FNA again do not give a cast-iron diagnosis. Our patient had a symptomatic cystic lesion in his pancreas which was excised after cross-specialty discussion. We advocate that this is the ideal way to treat patients with cystic lesions of the pancreas, with each case considered on its own merits as all current diagnostic investigations have their limitations.

scholarly journals Vallecular cyst in an infant with stridor: a case report

2018 ◽  
Vol 6 (1) ◽  
pp. 58-62
Author(s):  
Nabin Lageju ◽  
Rajendra Prasad Sharma Guragain
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Cystic Lesion ◽  
Failure To Thrive ◽  
Surgical Excision ◽  
Infants And Children ◽  
Solid Component ◽  
Feeding Difficulties ◽  
The Right ◽  
In Infants And Children

Background and Objectives: Vallecular cysts are rare and generally asymptomatic. In infants and children they present with stridor, feeding difficulties, failure to thrive. Treatment is surgical excision with cautery or laser.Presentation of Case: We discuss the clinical, radiological presentation of a 7 months old child with vallecular cyst which was surgically treated with deroofing and marsupialisation with elecrocautery. There was no recurrence even up 2 years of follow-up.Discussion: Flexible nasopharyngolaryngoscopic examination was done which showed present of swelling in the left vallecula pushing the epiglottis posteriorly and to the right with narrowed normal endolarynx. Radiological investigations with CT scan showed cystic lesion noted in left side of neck with no septation and solid component. The lesion was extending to ipsilateral vallecula and paraglottic region with narrowing of endolarynx.Conclusion: Vallecular cyst is rare cause of noisy breathing in infants and children. In adults it is usually asymptomatic. Treatment of choice is marsupialization with electrocautery or laser.

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