Literature DB >> 21487550

Squamous cell carcinoma of the descending colon: report of a case and literature review.

Hidenori Miyamoto1, Masanori Nishioka, Nobuhiro Kurita, Junko Honda, Kouzou Yoshikawa, Jun Higashijima, Tomohiko Miyatani, Yoshimi Bandou, Mitsuo Shimada.   

Abstract

It is very rare that squamous cell carcinoma (SCC) arises from colorectal epithelium. An 89-year-old man was treated in 2001 with chief complaints of anorexia, abdominal pain, and low grade fever. The histological diagnosis as SCC was determined by biopsy during a colonoscopy. We diagnosed primary SCC of the colon because except in the colon no malignant lesions were found by systemic CT. Surgical complete resection was performed. However, he died three months after surgical resection because of hepatic metastasis and cachexia. The prognosis of this disease seems to be worse than that of adenocarcinoma.

Entities:  

Keywords:  Colon; Prognosis; Squamous cell carcinoma

Year:  2007        PMID: 21487550      PMCID: PMC3073792          DOI: 10.1159/000107470

Source DB:  PubMed          Journal:  Case Rep Gastroenterol        ISSN: 1662-0631


Introduction

It is well known that more than 90% of colorectal diseases are adenocarcinoma, with the majority of remaining cases having no epithelial histology such as carcinoid tumors, sarcomas, and lymphoid tumors [1]. Pure squamous cell carcinoma (SCC) is not uncommon in glandular organs such as the uterus, lung, and pancreas, but a tumor of the intestinal tract is rare [2]. The incidence of SCC of the colon and rectum has been reported to be 0.25 to 0.1 per 1,000 colorectal carcinomas [3]. After the first case report in 1919 [4], a total 72 pure SCCs of the colon and rectum have been reported [3, 5, 6, 7]. Clinical characteristics, biologic behavior, and treatment response of this colorectal cancer are largely unknown. In this paper we report a case of primary SCC of the descending colon.

Case Report

An 89-year-old man underwent surgical operation for sigmoid colon cancer in 1994. Histological feature was well differentiated adenocarcinoma. He visited our hospital with low grade fever, anorexia and abdominal pain, seven years after the first operation in May 2001. Abdominal examination revealed a mass in the left upper quadrant. Barium enema showed irregular stenosis of the colon at the splenic flexure. Abdominal computed tomography (CT) showed wall thickness and stenosis of the colon at the splenic flexure and lymph node enlargement around the tumor (fig. 1). Colonoscopy revealed stenosis with ulceration in the colon at the splenic flexure. The histological diagnosis of SCC was determined by biopsies during colonoscopy. Although chest, neck and cervical CT were done, tumors were only identified in the colon. Therefore, we concluded that the colon was the primary lesion site. Although this tumor was a huge mass which penetrated the jejunum and adhered to the left kidney and left diaphragm, left hemicolectomy, partial resection of the jejunum and splenectomy were performed. The resected mass was huge, 11.0 × 8.0 cm, with penetration to the jejunum (fig. 2). Pathology demonstrated SCC of the colon at the splenic flexure invading the jejunum, diaphragm and capsule of the kidney (fig. 3a). Regional lymph nodes had metastasis of SCC (fig. 3b). A curative operation was performed. Adjuvant chemotherapy was not started because of the advanced age of the patient. Three months after the operation he died because of multiple liver metastases and cachexia.
Fig. 1

Abdominal computed tomography (CT) scan showed a large heterogeneous mass involving the colon at the splenic flexure and swelling lymph nodes.

Fig. 2

Macroscopic appearance. The resected specimen was a huge mass of 11.0 × 8.0 cm.

Fig. 3

a Primary tumor showing weak squamous change, demonstrating moderately differentiated SCC. Original magnification ×100. HE stain. b Metastatic lymph node showing metastatic, moderately differentiated SCC. Original magnification ×100. HE stain.

Discussion

SCCs of the colon are an extremely rare clinical entity. The first case of a pure SCC of the colon was reported in the German literature by Schmidtmann in 1919 [4]. In Japan, Murakami et al. reported the first case of a pure SCC of the colon in 1974 [8]. Since that initial description 72 cases of pure SCCs of the colon and rectum have been reported (table 1) [3, 5, 6, 7].
Table 1

Squamous cell carcinoma of the colon and rectum: clinical feature

Case Author (year)Age yearsGenderLocationTreatmentOutcome
1Schmidtmann (1919)65McecumDOD at 1 month
2Catell and Williams (1943)63Mrectum at 10 cmsurgical resectionalive at 3.5 years
3Hicks and Cowling (1955)90Fascending colonN/ADOD at 1 month
4Wiener et aL (1962)52Frectum at 9 cmAPRdied at 1 year
5Larizaden and Powell (1965)44Fhepatic flexureright hemicolectomyalive at 8 months
6Wood (1967)58Mcecumright hemicolectomyN/A
7Minkowitz (1967)49Frectosigmoidproctocolectomydead at 5 months
8Gaston (1967)65Mcecumright hemicolectomyalive at 2 years
9Pemberton and Lendrum (1968)48Fascending colonright hemicolectomyalive at 2 years
10Birnbaum (1970)82Mascending colonright hemicolectomyN/A
11Comer et al. (1971)34Frectum at 8 cmAPRalive at 13 years
12transverse colon
13descending colon
14upper rectum
15ascending colon
16hepatic flexure
17sigmoid
18sigmoid
19Lewis et al. (1971)61Mcecumright hemicolectomydead at 10 days
20Balfour (1972)63Msigmoidalive at 18 months
21Home and McCulloch (1978)53Mcecumright hemicolectomydead at 11 months
22Crissman (1978)72Mtransverse coloncolectomydead at 3 days
23Burgess et al. (1979)43Mhepatic flexureright hemicolectomydead at 1 year
24Williams et al. (1979)N/AN/ArectumN/AN/A
25Kahn et al. (1979)64Mascending colonN/AN/A
26Hickey and Corson (1981)48Ftransverse colontransverse/left hemicolectomyalive at 21 months
27Petrelli et al. (1981)73Msigmoidpalliative colostomydead at 9 days
28Pitella and Torres (1982)33Mascending colonileocolic bypassdead at 10 days
29Hey and Brandt (1982)N/AN/Acolon (not specified)N/AN/A
30N/AN/Acolon (not specified)N/AN/A
31Lyttle (1983)65Fascending colonright hemicolectomyalive at 2 months
32Vezeridis et al. (1983)56Mrectum at 10 cmAPRintraoperative death
3357Mtransverse coloncolectomyalive at 14 months
3444MrectumAPRdead at nine days
3561Frectuminvestigational chemotherapydead at 4 months
3666Frectum at 5 cm5-FU and radiationdead at 15 months
3762FrectumAPRdead at 13 months
38Gould et al. (1983)61Msplenic flexureileocolic bypassdead at 3 months
39Francioni et al. (1983)N/AN/Acolon (not specified)N/AN/A
40Forouhar (1984)N/AN/Acolon (not specified)N/AN/A
41Balsano (1985)65Mcecumright hemicolectomyN/A
4258Mascending colonright hemicolectomyN/A
43Chulia et al. (1986)hepatic flexure
44Navarro et al. (1986)colon
45colon
46colon
47Pigott and Williams (1987)rectumAPRdoing well
48Shao et al. (1987)ascending colonright hemicolectomy
49Lundquest et al. (1988)cecum
50McMahon (1991)Ftransverse colon
51Wyatt (1991)71Mcecumalive at 1 year
52Schneider et al. (1992)rectumsurgery and RT
53rectumsurgery and RT
54rectumsurgery and RT
55Betancourt et al. (1992)hepatic flexure
56Vignale (1993)69Msigmoid colonalive at 8 months
57Yoshida et al. (1994)51Msplenic flexureleft hemicolectomydead 39 days after diagnosis
58Vraux et al. (1994)colonchemotherapydead 5 years after diagnosis
59Alekseev et al. (1994)colon
60Morita (1995)57Mascending colonalive at 2 years
61Petrelli et al. (1996)62MrectumAPR
6241Fcecumcolectomy
63Juturi et al. (1998)61Fhepatic flexureright hemicolectomyalive NED 18 years after diagnosis
6467MSigmoid colonleft hemicolectomy and CTdead of disease 15 months after diagnosis
65Goodfellow et al. (1999)66Mhepatic flexureright hemicolectomyN/A
66Copur et al. (2001)54MrectosigmoidAPR + CTdead at 18 months after diagnosis
67Gelas et al. (2002)47FrectumAPR + CT
6863MrectumAPR + CT
6970FrectumAPR
7093MrectumRT
7145Frectumlow anterior resection
7243Frectumlow anterior resection
73our case89Mdescending colondescending colectomydead 3 months after operation

N/A = Not available; DOD = died of disease; APR = abdominoperineal resection; 5-FU = 5-fluorouracil; RT = radiation therapy; CT = chemotherapy; NED = no evidence of disease.

Certain criteria must be satisfied before a diagnosis of primary SCC of the colon is made [9]. First, metastasis from other sites to the bowel must be ruled out. Second, a squamous-lined fistulous tract must not involve the affected bowel, because this may be a source of SCCs. Third, SCCs of the anus with proximal extension must be excluded. Fourth, SCC must be confirmed by histological analysis. Our case satisfied all these criteria. The prognosis of patients with colorectal SCC is difficult to establish because of the rarity of these tumors. The colorectal SCC seems to be more frequently locally invasive and more likely to involve regional lymphatics than the adenocarcinomas, probably because of a delayed diagnosis. In this case, the tumor was pT4 (invasion of the diaphragm and capsule of the kidney) and lymph node involvement. However, curative resection with a negative resection margin was performed. Comer et al. [10] suggested a poorer prognosis for patients with colorectal SCC than adenocarcinoma. The role of adjuvant chemotherapy or radiation remains unknown. Gelas et al. [3] reported that surgical resection after neoadjuvant combination of chemotherapy and external beam radiation therapy was useful for rectal SCC. Juturi et al. [5] reported that combination of cisplatin, 5-fluorouracil, and leucovorin would be a possible treatment option for patients with metastatic colorectal SCC. Copur et al. [7] reported that cisplatin, etoposide and 5-fluorouracil combination chemotherapy was effective and serum SCC antigen level was a useful marker of response to chemotherapy. Chemotherapy for colorectal SCC has been controversial. Nowadays, we think that surgical resection may be the first choice and adjuvant treatment (chemotherapy or radiation therapy) may be done if the patient has a good performance status. In conclusion, advanced colorectal SCC with invasion to adjacent organs and metastatic lymph nodes had a poor prognosis. Treatment selection is difficult because colorectal SCC is a very rare disease. However, surgical resection and adjuvant chemotherapy is a better approach to the treatment of colorectal SCC.
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