PS02.025: CHARACTERISTICS OF SUPERFICIAL BASALOID SQUAMOUS CELL CARCINOMA TREATED BY ENDOSCOPIC RESECTION

2018 ◽  
Vol 31 (Supplement_1) ◽  
pp. 127-127
Author(s):  
Tsuneo Oyama ◽  
Akiko Takahashi

Abstract Background Basaloid squamous cell carcinoma (BSCC) is a rare esophageal carcinoma. And the characteristics especially in early stage is unknown. Methods The aim of this study is to clarify the characteristics of superficial BSCC. Thirteen patients (9 males and 4 females) with BSCC treated by endoscopic resection (12 ESD and 1 EMRC) from January 2000 to March 2017 were enrolled in this retrospective study. The median age was 67 (57–83). The median follow-up period was 24 (12–115) months. T1a-EP/LPM and T1a-MM/T1b-SM1 without lymph duct invasion (LDI) was followed up. T1a-MM/T1b-SM1 with LDI or T1b-SM2 were treated by additional treatment (AT). Results 1. En-bloc resection and R0 resection rate was 100% and 100%, respectively. 2. Macroscopic type; 0-IIa, 0-IIb and 0-IIc was 4, 1 and 8, respectively. 3. The median tumor diameter was 27 (2–62) mm. 4. Invasion depth; T1a-LPM, T1a-MM/T1b-SM1, and T1b-SM2 was 3, 5 and 5, respectively. 5. Histological characteristics; All BSCC were covered by SCC or non-neoplastic squamous epithelium. 6. Endoscopic characteristics; SMT like appearance was found in 46% (6/13). Yellowish nodules were observed in 23% (3/13). This finding was observed, when BSCC exist superficial epithelial layer covered by thin non-neoplastic epithelium. 7. Prognosis A: T1a-LPM (N = 3). Two patients are alive without recurrence, and 1 patient died of other disease. B: T1a-MM/SM1 (N = 5). Two of 3 patients without LDI were followed up and alive. Remaining one patient wanted to be treated by CRT, and alive. Two patients had LVI, however they were followed up without AT because of patient's hope. One is alive, and another died of other disease. C: T1b-SM2 (N = 5). Two and one patients were treated by surgery and chemotherapy, respectively, and alive without recurrence. Remaining two patients were followed up without AT. One of 2 patients are alive without recurrence. Another patient dead of other disease. Conclusion 1. All of BSCC were covered by SCC or non-neoplastic epithelium. 2. SMT like appearance and yellowish nodules under squamous cell epithelium were the characteristic endoscopic findings. 3. 40% of T1aMM/T1bSM1 had LDI. It's higher than that of SCC. Therefore, En-bloc resection is necessary for the detailed histological examination. Disclosure All authors have declared no conflicts of interest.

2015 ◽  
Vol 62 (3) ◽  
pp. 801-802
Author(s):  
Eric B. Trestman ◽  
Pablo De Los Santos ◽  
Evan Garfein ◽  
Thomas Ow ◽  
Evan C. Lipsitz ◽  
...  

1999 ◽  
Vol 123 (11) ◽  
pp. 1115-1117 ◽  
Author(s):  
Dan J. Vick ◽  
Zachary D. Goodman ◽  
Kamal G. Ishak

Abstract Ciliated hepatic foregut cysts are rare congenital lesions derived from the embryologic foregut. They are considered benign, and a review of 64 published cases revealed no instances of malignant transformation. We report a case of squamous cell carcinoma arising in a ciliated hepatic foregut cyst in a 51-year-old man. The tumor was found during a routine cholecystectomy and involved the adjacent mesentery and duodenal wall. There was histologic evidence of perineural and perivascular involvement. Despite an en bloc resection of the tumor and contiguous areas of gross involvement, the patient died 2 months later. Although aspiration of cyst contents is an accepted treatment for asymptomatic lesions, this case suggests that most ciliated hepatic foregut cysts should be excised, especially when radiologic studies yield equivocal results.


1999 ◽  
Vol 75 (2) ◽  
pp. 282-284 ◽  
Author(s):  
Lawrence R. Nycum ◽  
John H. Farley ◽  
Mark E. Reed ◽  
Robert R. Taylor

Toukeibu Gan ◽  
2011 ◽  
Vol 37 (3) ◽  
pp. 349-354
Author(s):  
Hiroki Mitani ◽  
Kazuyoshi Kawabata ◽  
Hiroyuki Yonekawa ◽  
Hirofumi Fukushima ◽  
Tohru Sasaki ◽  
...  

2021 ◽  
pp. 58-59
Author(s):  
Hitesh Soni ◽  
Saurabh Kalia ◽  
J M Mehta ◽  
Manisha Agarwal

Primary squamous cell carcinoma at ileostomy site is extremely rare and there are only eight reported cases prior to our report. The present case report describes a patient of ileostomy formation 12 years prior to evaluation after total colectomy who now presented with mass at stomal and parastomal site and underwent biopsy and Positron emission tomography (PET) scan. Tumor was suspected and hence wide local excision with en bloc resection of the ileostomy and ileo-rectal anastomosis was done and histopathology showed differentiated Squamous cell carcinoma (SCC), Grade 1. This case underlines the need of regular follow-up of patients with stomas to allow the timely detection of stomal problems and the early diagnosis and management of the rare complication of parastomal squamous-cell carcinoma. Also, persistent peristomal ulcerations and proliferative lesions must undergo biopsies to rule out malignancy. Wide local excision of the carcinoma with en bloc resection of ileostomy and formation of new ileostomy at a different site is usually done to manage such cases.


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