Case Report September 2014

Lipoma Arborescens of The Knee: A Case Report

Case Report September 2014 107 Views

Lipoma Arborescens is a rare intra-articular tumor. Knee is the most commonly affected joint, whereas ankle, hip, shoulder and elbow may be involved. There are few case reports published in the literature. We report a case with lipoma arborescens in the knee joint to improve the medical knowledge about the pathology and management of this rare entitiy. 20-year-old Caucasian female…

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Recieved 05.11.2011
Accepted 13.12.2011
Published Online 13.12.2011
Printed 01.09.2014
DOI 10.4328/JCAM.847
Author Mehmet Erdil, Yunus Imren, Kerem Bilsel, Hasan Huseyin Ceylan, Ibrahim Tuncay
Identifier J Clin Anal Med. 2014;5(5):429-431
Index Page 429-431
Citations in Google Scholar Google Scholar
How to Cite Mehmet Erdil, Yunus Imren, Kerem Bilsel, Hasan Huseyin Ceylan, Ibrahim Tuncay. Lipoma Arborescens of The Knee: A Case Report. J Clin Anal Med. 2014;5(5):429-431
Running Title Lipoma Arborescens

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KATD-847.pdf

Angiosarcoma of the Thyroid and Regional Lymph Node Metastasis

Case Report September 2014 111 Views

Thyroid angiosarcomas are typically infiltrative and large tumors with very similar clinical findings of anaplastic carcinoma of thyroid. Early hematogenous metastasis is very frequent, but regional lymph node metastasis is quite rare. We present a case of angiosarcoma of the thyroid gland in a 68 years old man with regional lymph node metastasis. Total thyroidectomy with right modified radical neck…

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Recieved 14.10.2011
Accepted 07.12.2011
Published Online 07.12.2011
Printed 01.09.2014
DOI 10.4328/JCAM.828
Author Lutfi Dogan, Niyazi Karaman, Cigdem Irkkan, Ali Kucuk, Can Atalay
Identifier J Clin Anal Med. 2014;5(5):426-428
Index Page 426-428
Citations in Google Scholar Google Scholar
How to Cite Lutfi Dogan, Niyazi Karaman, Cigdem Irkkan, Ali Kucuk, Can Atalay. Angiosarcoma of the Thyroid and Regional Lymph Node Metastasis. J Clin Anal Med. 2014;5(5):426-428
Running Title Angiosarcoma of the Thyroid and Metastasis

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KATD-828.pdf

Inflamatuar Psedotumor of the Bladder: A Case Report And Review of the Literature

Case Report September 2014 113 Views

The most of bladder tumors are urothelial carcinomas. Inflammatory pseudotumoris a benign non epithelial rare tumor in the urinary bladder. A 25-years-old pregnant female admitted to our clinic with a complaint of dysuria and macroscopic hematuria. Ultrasongraphy, revealed a 4x3 cm broad-based solitary bladder tumor localized in the posterior wall of the urinary bladder. The clinical diagnosis was bladder tumor…

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Recieved 28.09.2011
Accepted 17.11.2011
Published Online 17.11.2011
Printed 01.09.2014
DOI 10.4328/JCAM.818
Author Adem Yasar, Yusuf Gencten, Fatih Firat, Fatma Markoc, Fikret Erdemir
Identifier J Clin Anal Med. 2014;5(5):423-425
Index Page 423-425
Citations in Google Scholar Google Scholar
How to Cite Adem Yasar, Yusuf Gencten, Fatih Firat, Fatma Markoc, Fikret Erdemir. Inflamatuar Psedotumor of the Bladder: A Case Report And Review of the Literature. J Clin Anal Med. 2014;5(5):423-425
Running Title Inflammatory Pseudotumor of the Bladder

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KATD-818.pdf

Pseudomyxoma Peritonei Secondary to Apendix Malign Musinous Tumour; Case Report

Case Report September 2014 122 Views

Most cases of pseudomyxoma peritonei are caused by appendiceal musinous tumor. It is diagnosis remains challencing to most clinicians. There is still some debate about treatment. New treatment methods can achieve satisfactory results in patients with PMP. In this report, we present a case with pseudomyxoma peritonei origin from appendix mucinous tumor.

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Recieved 26.09.2011
Accepted 09.11.2011
Published Online 09.11.2011
Printed 01.09.2014
DOI 10.4328/JCAM.791
Author Burhan Mayir
Identifier J Clin Anal Med. 2014;5(5):420-422
Index Page 420-422
Citations in Google Scholar Google Scholar
How to Cite Burhan Mayir. Pseudomyxoma Peritonei Secondary to Apendix Malign Musinous Tumour; Case Report. J Clin Anal Med. 2014;5(5):420-422
Running Title Pseudomyxoma Peritonei

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KATD-791.pdf

Presacral Schwannoma: A Case Report

Case Report September 2014 87 Views

Schwannomas are encapsulated peripheral nerve sheath tumors. They are rarely seen in the presacral area and are reported mostly in women. Complete resection is mandatory for treatment of schwannoma. After surgical resection recurrence is rare, and the prognosis is usually good. A 34 years old woman with presacral schwannoma who is successfully treated via transabdominal total excision is presented here…

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Recieved 23.10.2011
Accepted 23.10.2011
Published Online 23.10.2011
Printed 01.09.2014
DOI 10.4328/JCAM.823
Author Alper Bilal Ozkardes, Mehmet Tokac, Fahri Yetisir, Birkan Bozkurt, Mehmet Kilic
Identifier J Clin Anal Med. 2014;5(5):417-419
Index Page 417-419
Citations in Google Scholar Google Scholar
How to Cite Alper Bilal Ozkardes, Mehmet Tokac, Fahri Yetisir, Birkan Bozkurt, Mehmet Kilic. Presacral Schwannoma: A Case Report. J Clin Anal Med. 2014;5(5):417-419
Running Title Presacral Schwannoma

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KATD-823.pdf