scholarly journals Postoperative recurrence of myxoid liposarcoma of left thigh with pericardial metastasis: A case report

2021 ◽  
Author(s):  
Wenpeng Huang ◽  
Jianbo Gao ◽  
Liming Li
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Myxoid Liposarcoma ◽  
Postoperative Recurrence ◽  
Left Thigh ◽  
Cardiac Abnormality ◽  
Pericardial Cyst ◽  
Pericardial Metastasis

We report a rare case of postoperative recurrence of MLS in the left thigh with ectopic and metachronous pericardial metastases. He was found to have a cardiac abnormality that was initially thought to be a pericardial cyst, but was later pathologically confirmed to be MLS metastasis.

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.

scholarly journals Myxoid liposarcoma with metastasis to the pancreas: a rare case report and review of the literature

2020 ◽  
Author(s):  
Ankang Wang ◽  
Peng Cong ◽  
Zhenxing He ◽  
Yueyu Qu ◽  
Tao Hu ◽  
...  
Keyword(s):  
Case Report ◽  
Gastrointestinal Bleeding ◽  
Rare Case ◽  
Radical Surgery ◽  
Myxoid Liposarcoma ◽  
Review Of The Literature ◽  
Case Presentation ◽  
Complete Surgical Resection ◽  
Rare Case Report ◽  
Rare Malignancy

Abstract BackgroundMetastasis of the pancreas to myxoid liposarcoma is very rare.Case presentationWe report a 43-year-old woman who underwent radical surgery for myxoid liposarcoma (MLPS) of the sigmoid colon 9 years earlier and for liposarcoma of the neck 7 years earlier. The lesion later metastasized to the pancreas, and we performed pancreaticoduodenectomy, which was pathologically confirmed as myxoid liposarcoma. Unfortunately, the patient died a year later from unexplained gastrointestinal bleeding.ConclusionsMyxoid liposarcoma is a very rare malignancy that carries a risk of invasion to the pancreas, and complete surgical resection is the best chance for clinical treatment.

scholarly journals MYXOID LIPOSARCOMA OF THE SPERMATIC CORD M IMICKING LEFT INGUINAL HERNIA : A RARE CASE REPORT

2015 ◽  
Vol 4 (96) ◽  
pp. 16198-16200
Author(s):  
Sanjay Nigam ◽  
Shalini Shukla ◽  
Neha Ahuja ◽  
Jayant Rai ◽  
Parul Joshi
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Case ◽  
Myxoid Liposarcoma ◽  
Rare Case Report

scholarly journals Nevus Comedonicus, a Rare Case : Dermoscopic and Histopathological Findings

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Nugrohoaji Dharmawan ◽  
Endra Yustin Ellistasari ◽  
Oyong Oyong ◽  
Adniana Nareswari
Keyword(s):  
Case Report ◽  
Diagnostic Tool ◽  
Rare Case ◽  
Histopathological Examination ◽  
Left Thigh ◽  
Hypertrophic Scars ◽  
Distinctive Pattern ◽  
Linear Pattern ◽  
Non Invasive ◽  
Blaschko’S Lines

Nevus comedonicus is an extremely rare adnexal hamartoma of pilosebaceous apparatus, with approximately 200 cases reported in the literature so far. It appears as cluster of adjacent honeycomb-like dillated follicular openings with firm pigmented keratin plugs resembling comedones.The comedones oftentimes arranged in linear pattern paralled to Blaschko’s lines. We report a case of a 5-year-old boy with open brown to black comedones in a linear pattern localized on the back of the left thigh that appearing since birth. Pain, itch and discharge were not obtain. There were some episodes of infection, due to manual removal done by his mother which left some hypertrophic scars. Dermoscopic examination revealed the distinctive pattern consisting of pigmented, sharply demarcated keratin plugs of 1-3 mm in diameter, some open pores, multiple structurless, various shades of brown homogenous circular areas surrounding the plugs. Histopathological examination showed an aggregation of dilated follicular infundibulum with laminated keratinous material plugging. This case report prove that dermoscopy examination, a simple non-invasive diagnostic tool is very helpful in diagnosing nevus comedonicus. We recommend this tool to differentiate the diagnosis of other rare epidermal nevi while histopathological examination should be performed only in uncertain cases.

scholarly journals Woolly hair with palmoplantar keratoderma without cardiac abnormality: A rare case report

2020 ◽  
Vol 21 (1) ◽  
pp. 47
Author(s):  
Saritha Mohanan ◽  
Alagammai Krishnappan ◽  
Udayashankar Carounanidhi ◽  
RamachandranV Bhat
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cardiac Abnormality ◽  
Palmoplantar Keratoderma ◽  
Rare Case Report ◽  
Woolly Hair

scholarly journals Cardiac Tamponade by Hydatid Pericardial Cyst: A Rare Case Report

2013 ◽  
Vol 3 (3) ◽  
Author(s):  
Anil Kumar Paswan ◽  
Shashi Prakash ◽  
Rajeev K Dubey
Keyword(s):  
Case Report ◽  
Cardiac Tamponade ◽  
Rare Case ◽  
Pericardial Cyst ◽  
Rare Case Report

scholarly journals Multiple Warthin Tumors With Epithelial–Myoepithelial Carcinoma of the Ipsilateral Parotid Gland: A Case Report

2021 ◽  
pp. 014556132110280
Author(s):  
Tong Sha ◽  
Yang Yu ◽  
Kang Liu ◽  
Bin Sun ◽  
Wei Zhang
Keyword(s):  
Case Report ◽  
Parotid Gland ◽  
Rare Case ◽  
Malignant Tumors ◽  
Postoperative Recurrence ◽  
Myoepithelial Carcinoma ◽  
Primary Tumors ◽  
Multiple Primary Tumors ◽  
Multiple Primary ◽  
Epithelial Myoepithelial Carcinoma

Multiple primary tumors of the parotid gland refer to the occurrence of 2 or more primary tumors in the ipsilateral or bilateral parotid gland metachronously or synchronously, which do not originate from postoperative recurrence or metastasis. Multiple primary tumors of the parotid gland, especially synchronous benign and malignant tumors, are extremely uncommon. A rare case of multiple Warthin tumors with epithelial–myoepithelial carcinoma of the ipsilateral parotid gland is reported as follows.

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