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. 2007 Aug 29;1(1):77–83. doi: 10.1159/000107470

Squamous Cell Carcinoma of the Descending Colon: Report of a Case and Literature Review

Hidenori Miyamoto a,*, Masanori Nishioka a, Nobuhiro Kurita a, Junko Honda a, Kouzou Yoshikawa a, Jun Higashijima a, Tomohiko Miyatani a, Yoshimi Bandou b, Mitsuo Shimada a
PMCID: PMC3073792  PMID: 21487550

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.

Key Words: Squamous cell carcinoma, Colon, Prognosis

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.

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.

Fig. 2

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

Fig. 3.

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 years Gender Location Treatment Outcome
1 Schmidtmann (1919) 65 M cecum DOD at 1 month
2 Catell and Williams (1943) 63 M rectum at 10 cm surgical resection alive at 3.5 years
3 Hicks and Cowling (1955) 90 F ascending colon N/A DOD at 1 month
4 Wiener et aL (1962) 52 F rectum at 9 cm APR died at 1 year
5 Larizaden and Powell (1965) 44 F hepatic flexure right hemicolectomy alive at 8 months
6 Wood (1967) 58 M cecum right hemicolectomy N/A
7 Minkowitz (1967) 49 F rectosigmoid proctocolectomy dead at 5 months
8 Gaston (1967) 65 M cecum right hemicolectomy alive at 2 years
9 Pemberton and Lendrum (1968) 48 F ascending colon right hemicolectomy alive at 2 years
10 Birnbaum (1970) 82 M ascending colon right hemicolectomy N/A
11 Comer et al. (1971) 34 F rectum at 8 cm APR alive at 13 years
12 transverse colon
13 descending colon
14 upper rectum
15 ascending colon
16 hepatic flexure
17 sigmoid
18 sigmoid
19 Lewis et al. (1971) 61 M cecum right hemicolectomy dead at 10 days
20 Balfour (1972) 63 M sigmoid alive at 18 months
21 Home and McCulloch (1978) 53 M cecum right hemicolectomy dead at 11 months
22 Crissman (1978) 72 M transverse colon colectomy dead at 3 days
23 Burgess et al. (1979) 43 M hepatic flexure right hemicolectomy dead at 1 year
24 Williams et al. (1979) N/A N/A rectum N/A N/A
25 Kahn et al. (1979) 64 M ascending colon N/A N/A
26 Hickey and Corson (1981) 48 F transverse colon transverse/left hemicolectomy alive at 21 months
27 Petrelli et al. (1981) 73 M sigmoid palliative colostomy dead at 9 days
28 Pitella and Torres (1982) 33 M ascending colon ileocolic bypass dead at 10 days
29 Hey and Brandt (1982) N/A N/A colon (not specified) N/A N/A
30 N/A N/A colon (not specified) N/A N/A
31 Lyttle (1983) 65 F ascending colon right hemicolectomy alive at 2 months
32 Vezeridis et al. (1983) 56 M rectum at 10 cm APR intraoperative death
33 57 M transverse colon colectomy alive at 14 months
34 44 M rectum APR dead at nine days
35 61 F rectum investigational chemotherapy dead at 4 months
36 66 F rectum at 5 cm 5-FU and radiation dead at 15 months
37 62 F rectum APR dead at 13 months
38 Gould et al. (1983) 61 M splenic flexure ileocolic bypass dead at 3 months
39 Francioni et al. (1983) N/A N/A colon (not specified) N/A N/A
40 Forouhar (1984) N/A N/A colon (not specified) N/A N/A
41 Balsano (1985) 65 M cecum right hemicolectomy N/A
42 58 M ascending colon right hemicolectomy N/A
43 Chulia et al. (1986) hepatic flexure
44 Navarro et al. (1986) colon
45 colon
46 colon
47 Pigott and Williams (1987) rectum APR doing well
48 Shao et al. (1987) ascending colon right hemicolectomy
49 Lundquest et al. (1988) cecum
50 McMahon (1991) F transverse colon
51 Wyatt (1991) 71 M cecum alive at 1 year
52 Schneider et al. (1992) rectum surgery and RT
53 rectum surgery and RT
54 rectum surgery and RT
55 Betancourt et al. (1992) hepatic flexure
56 Vignale (1993) 69 M sigmoid colon alive at 8 months
57 Yoshida et al. (1994) 51 M splenic flexure left hemicolectomy dead 39 days after diagnosis
58 Vraux et al. (1994) colon chemotherapy dead 5 years after diagnosis
59 Alekseev et al. (1994) colon
60 Morita (1995) 57 M ascending colon alive at 2 years
61 Petrelli et al. (1996) 62 M rectum APR
62 41 F cecum colectomy
63 Juturi et al. (1998) 61 F hepatic flexure right hemicolectomy alive NED 18 years after diagnosis
64 67 M Sigmoid colon left hemicolectomy and CT dead of disease 15 months after diagnosis
65 Goodfellow et al. (1999) 66 M hepatic flexure right hemicolectomy N/A
66 Copur et al. (2001) 54 M rectosigmoid APR + CT dead at 18 months after diagnosis
67 Gelas et al. (2002) 47 F rectum APR + CT
68 63 M rectum APR + CT
69 70 F rectum APR
70 93 M rectum RT
71 45 F rectum low anterior resection
72 43 F rectum low anterior resection
73 our case 89 M descending colon descending colectomy dead 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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