Tattoo of colonic neoplasms in 113 patients with a new sterile carbon compound

2002 ◽  
Vol 56 (3) ◽  
pp. 339-342 ◽  
Author(s):  
Matthew P. Askin ◽  
Jerome D. Waye ◽  
Lawrence Fiedler ◽  
Noam Harpaz
2002 ◽  
Vol 56 (3) ◽  
pp. 339-342 ◽  
Author(s):  
Matthew P. Askin ◽  
Jerome D. Waye ◽  
Lawrence Fiedler ◽  
Noam Harpaz

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Akihiro Yoshida ◽  
Yasutake Uchima ◽  
Naoki Hosaka ◽  
Kosuke Minaga ◽  
Masatoshi Kudo

Abstract Background Colonic volvulus, a condition in which a colonic segment partially twists around its base, is the third leading cause of large bowel obstruction after colonic neoplasms and diverticular disease. However, volvulus of the transverse colon is the rarest type of large intestinal volvulus. Moreover, the occurrence of transverse colonic volvulus secondary to a benign tumor originating from outside the intestine has never been reported. We hereby report a case of transverse colonic volvulus caused by mesenteric fibromatosis. Case presentation A 53-year-old female with a history of rheumatoid arthritis and thyroid tumor presented with abdominal pain for 1 day. Abdominal computed tomography revealed intestinal torsion at the hepatic flexure. Twisted and obstructed mucosa of the transverse colon was observed during colonoscopy, but no tumor invasion of the mucosal surface was detected. A solid mass of a mesenteric origin with involvement of the transverse colon was observed during surgery. The mass was diagnosed surgically as transverse colonic volvulus induced by a mesenteric tumor. Hence, the patient underwent a right hemicolectomy. Histopathological results indicated mesenteric desmoid-type fibromatosis. The postoperative recovery was uneventful, and the patient was discharged 8 days after surgery. Conclusions Although mesenteric fibromatosis is rare, this disease should be considered when managing transverse colonic volvulus resulting from nonmucosal tumors.


Cases Journal ◽  
2009 ◽  
Vol 2 (1) ◽  
pp. 8317 ◽  
Author(s):  
Muhammad Imran Aslam ◽  
Imen Ben Salha ◽  
Salli Muller ◽  
John Stuart Jameson

Dermatology ◽  
1989 ◽  
Vol 178 (1) ◽  
pp. 23-28 ◽  
Author(s):  
Robert A. Schwartz ◽  
David J. Goldberg ◽  
Fayyaz Mahmood ◽  
Robert L. DeJager ◽  
Clark Lambert ◽  
...  
Keyword(s):  

1994 ◽  
Vol 40 (6) ◽  
pp. 777-778 ◽  
Author(s):  
Marco Pennazio ◽  
Arrigo Arrigoni ◽  
Francesco Paolo Rossini

2016 ◽  
Vol 28 (4pt2) ◽  
pp. 1413-1419 ◽  
Author(s):  
Dante Cicchetti ◽  
Susan Hetzel ◽  
Fred A. Rogosch ◽  
Elizabeth D. Handley ◽  
Sheree L. Toth

AbstractA genome-wide methylation study was conducted among a sample of 114 infants (M age = 13.2 months, SD = 1.08) of low-income urban women with (n = 73) and without (n = 41) major depressive disorder. The Illumina HumanMethylation450 BeadChip array with a GenomeStudio Methylation Module and Illumina Custom model were used to conduct differential methylation analyses. Using the 5.0 × 10–7p value, 2,119 loci were found to be significantly different between infants of depressed and nondepressed mothers. Infants of depressed mothers had greater methylation at low methylation sites (0%–29%) compared to infants of nondepressed mothers. At high levels of methylation (70%–100%), the infants of depressed mothers were predominantly hypomethylated. The mean difference in methylation between the infants of depressed and infants of nondepressed mothers was 5.23%. Disease by biomarker analyses were also conducted using GeneGo MetaCore Software. The results indicated significant cancer-related differences in biomarker networks such as prostatic neoplasms, ovarian and breast neoplasms, and colonic neoplasms. The results of a process networks analysis indicated significant differences in process networks associated with neuronal development and central nervous system functioning, as well as cardiac development between infants of depressed and nondepressed mothers. These findings indicate that early in development, infants of mothers with major depressive disorder evince epigenetic differences relative to infants of well mothers that suggest risk for later adverse health outcomes.


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