Home Print this page Email this page Users Online: 354
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login 

 Table of Contents  
Year : 2020  |  Volume : 27  |  Issue : 2  |  Page : 136-142

Socio-demographic and clinico-pathologic pattern of patients with colorectal cancers seen in Ahmadu Bello University Teaching Hospital, Zaria

1 Department of Radiology, Barau Dikko Teaching Hospital, Kaduna, Nigeria
2 Department of Radiotherapy and Oncology, Ahmadu Bello University Teaching Hospital, Zaria, Kaduna State, Nigeria
3 Department of Radiotherapy, Lagos University Teaching Hospital, Lagos, Lagos State, Nigeria, Nigeria<
4 Department of Radiology, Federal Medical Centre, Birnin Kebbi, Kebbi State, Nigeria

Date of Submission21-Jul-2019
Date of Acceptance25-Jul-2020
Date of Web Publication24-Sep-2020

Correspondence Address:
Dr. Hadiza Theyra-Enias
Department of Radiology, Barau Dikko Teaching Hospital, P. O. Box 9727, Lafiya Road, Kaduna, Kaduna State
Login to access the Email id

DOI: 10.4103/wajr.wajr_27_19

Rights and Permissions

Introduction: Colorectal cancer is a major cause of morbidity and mortality in the world. It accounts for 10.2% of cancer incidence globally, with a mortality of 9.2%. It ranks third in terms of incidence but second in terms of mortality. Colorectal cancer is not uniformly common throughout the world. Its incidence is increasing in developing countries, probably due to the acquisition of western lifestyle.
Aim: The aim of this study was to determine the sociodemographic and clinicopathological pattern of patients with colorectal cancer seen in the Department of Surgery, Radiotherapy, and Oncology Centre, Ahmadu Bello University Teaching Hospital (ABUTH), Zaria, over a 10-year period.
Materials and Methods: In this retrospective study, data were collected from the case files and treatment cards of 122 patients with colorectal cancer managed at the Surgical, Radiotherapy, and Oncology Department of ABUTH, Zaria, from January 2006 to December 2015. Data items analyzed included age, sex, residential area, occupation, duration of symptoms, presenting complaints, subsite, histological type, grade, and stage. All analyses were performed by SPSS version 20.
Results: An annual incidence of 12.2 cases/annum was seen. Seventy (57.4%) were male and 52 (42.6%) were female. Male:female ratio was 1.3:1 and the age range was between 12 years and 78 years, majority were between 31 and 40 years (24.6%), with a mean age of 42.4 years and median age of 41 years. It was found to be more common among the urban dwellers, with the public/civil servants being the most affected (36.0%). The duration of presenting complain ranged from 3 weeks to 10 years, most patients presenting at 7–10 months with more than one symptom. Bleeding per rectum was the most common symptom seen in 20%. Adenocarcinoma was the predominant histology seen in 73% (n = 89) and 28.7% were well differentiated. The rectum was the most common subsite, while left-sided lesions (20%) were more common than right-sided lesions (17%). About 18% (n = 22) had distant metastasis.
Conclusion: The study showed that colorectal cancer was more common among the younger age group, with a slight male preponderance. They were mostly urban dwellers and civil/public servants. The most common presenting symptom was bleeding per rectum and majority of the cases presented at an advanced stage. Early detection through public health education, screening programs, affordable and effective treatment, and follow-up will help reverse this trend.
Conclusion: The study showed that colorectal cancer was more common among the younger age group, with a slight male preponderance. They were mostly urban dwellers and civil/public servants. Bleeding per rectum being the most common complaint, majority of the cases presented at an advanced stage. Early detection through public health education, screening programs, affordable and effective treatment, and follow-up will help reverse this trend.

Keywords: Adenocarcinoma, age, colorectal cancer, Nigeria

How to cite this article:
Theyra-Enias H, Adewuyi SA, Alabi A, Jummai DJ, Zubairu IH. Socio-demographic and clinico-pathologic pattern of patients with colorectal cancers seen in Ahmadu Bello University Teaching Hospital, Zaria. West Afr J Radiol 2020;27:136-42

How to cite this URL:
Theyra-Enias H, Adewuyi SA, Alabi A, Jummai DJ, Zubairu IH. Socio-demographic and clinico-pathologic pattern of patients with colorectal cancers seen in Ahmadu Bello University Teaching Hospital, Zaria. West Afr J Radiol [serial online] 2020 [cited 2021 Apr 12];27:136-42. Available from: https://www.wajradiology.org/text.asp?2020/27/2/136/295944

  Introduction Top

Colorectal cancer is a major public health problem worldwide, representing a major cause of morbidity and mortality.[1] It accounts for over 10.2% of cancer incidence globally in both sexes. It is the third most common cancer worldwide and the second most common cause of death.[2] Worldwide, colorectal cancer represents 10.9% of all incident cancer in men and 9.5% in women.[2] Colorectal cancer, however, is not uniformly common throughout the world. Colorectal cancer is mainly a disease of developed countries with western culture.[3] The incidence rate varies up to 10-fold between countries with the highest rates and those with the lowest rates.[2]

In the developing countries, especially West Africa, the rate has not yet reached the magnitude of developed countries.[4] However, current publications indicate that the incidence is increasing in developing countries including sub-Saharan Africa, especially in the urban areas,[5] as seen in Ghana, Nigeria, Tunisia, and Egypt where it represents about 10%–50% of all malignant tumors.[5] In Nigeria, the incidence of colorectal cancer is put at 3.4/100,000 compared with 35.8/100,000 each year in the USA.[6] Colon and rectal carcinomas are not common in native Nigerians when compared to the incidence of this disease in the United States (US) and the United Kingdom (UK). Nevertheless, studies in Nigeria have shown increased rates of this disease over the past 20 years.[7]

The likelihood of colorectal cancer diagnosis increases progressively from age 40 years, rising sharply after age 50 years. More than 90% of colorectal cancer cases occur in people aged 50 years or older.[3] The incidence rate is more than 50 times higher in persons aged 60–79 years than in those younger than 40 years. However, colorectal cancer appears to be increasing among younger persons.[3] In the US, colorectal cancer is now one of the 10 most commonly diagnosed cancers among men and women aged 20–49 years.[3] The median age at colorectal cancer diagnosis in the US is 68 years in men and 72 years in women.[8] The risk factors for the development of colorectal cancer include both modifiable and nonmodifiable factors. The nonmodifiable risk factors include advance in age, genetic risks such as the familial adenomatous polyposis, hereditary nonpolyposis colorectal cancer (HNPCC also known as Lynch syndrome), family history of colorectal cancer, personal history of adenomatous polyps, and inflammatory bowel disease.[3] The non modifiable risk factors has a lot to do with environmental factors such as diet rich in animal fat, high meat consumption, diet low in fruits and vegetables, physical inactivity, obesity, cigarette smoking and alcohol consumption.[3]

There has been an unexplained shift in the natural history of colorectal cancer during the past 30-40 years,[9] although left sided colon cancers are still more common, several studies done showed proximal right ward shift.[10]

Tumors of the colorectum arise in the mucosa and are mostly (>90%) adenocarcinomas. Other histologic types include squamous cell carcinoma, carcinoid, leiomyosarcoma, and lymphoma. Most grading systems classify adenocarcinoma as well, moderately, or poorly differentiated.[11] Colorectal cancer often produces minimal or no symptoms. The clinical presentation of colorectal cancer is determined largely by the site of the tumor. Cancers of the right colon are often exophytic and commonly associated with iron deficiency anemia due to occult blood loss. Many of these are diagnosed late. Cancers of the left colon and sigmoid colon are often deeply invasive, annular, and accompanied by obstruction and rectal bleeding. Rectal cancer frequently results in bleeding and alterations in bowel habits.[11]

Colorectal cancer is a disease for which screening and preventive measures have proven effective in developed countries.[12] Primary preventive measures against colorectal cancer include: ingestion of diet rich in fiber which has a protective role and regular physical activity. The aim of screening is to reduce its incidence by detecting and re-sectioning precursor lesions and mortality by this cause.[13] Screening which consists of stool-based, imaging and endoscopic tests is widely used. Stool-based tests which include Guaiac-based fecal occult blood test (gFOBT) and fecal immunochemical test (FIT) can reduce mortality rates by early detection of asymptomatic cancerous lesions.[14] Imaging techniques such as computed tomographic colonography which is gaining popularity, colon capsule endoscopy, and double-contrast barium enema are used. Endoscopic tests include flexible sigmoidoscopy, colonoscopy which is considered the “gold standard” in colorectal cancer screening because of its high sensitivity and specificity for detecting precancerous and cancerous lesions.[14]

Guidelines from the American Society of Clinical Oncology and World Gastroenterology Organization recommend the use of gFOBT or FIT in an environment with limited endoscopic resources. In sub-Saharan Africa, there are no organized colorectal cancer screening projects or pilot projects, and in Nigeria, there is little evidence to suggest the efficacy and feasibility of gFOBT and FIT.[15]

However, in Nigeria despite the low incidence, the outcome of treatment still remains poor largely due to lack of screening, late presentation, ignorance, poverty, and superstition [6]. The aim of the study is to determine the sociodemographic and clinicopathological pattern of colorectal cancer seen in Ahmadu Bello University Teaching Hospital (ABUTH), Zaria, as comparable to documented cases in other regions.

  Materials and Methods Top

This study was carried out at the Surgical Outpatient Department and Radiotherapy and Oncology Department of ABUTH, Zaria. It is a tertiary institution located in Kaduna State, Northwest of Nigeria. The region has an average total population of 6,113,503 according to the Nigerian census figure, 2006.

It was a retrospective study; the case folders and surgical notes of all patients with histological diagnosis of colorectal cancer that were managed in either the surgical and or radiotherapy and oncology department of the institution over a 10 year period (January 2006–December 2015) were retrieved and studied. A total of 122 patients with a diagnosis of colorectal cancers were seen.

Definition of anatomical sites of colorectal cancer

  • Right sided: Lesions arising from the caecum, ascending colon, hepatic flexure, or transverse colon
  • Left sided: Lesions arising from the splenic flexure, descending colon, or sigmoid colon
  • Rectal: Rectosigmoid junction and rectal tumor
  • Colorectal cancer: It is a cancer that involves the large intestine, extending from the caecum to the rectum.

Inclusion criteria

Patients with histological diagnosis of colorectal cancer, who presented to either department of surgery or radiotherapy and oncology department between January 2006 and December 2015 were included in the study.

Exclusion criteria

  • Patients with benign diseases of the colon and rectum
  • Patients without a histological diagnosis of colorectal cancer
  • Staging system used was the Dukes' staging system.

Collected data were analyzed using the Statistical Package for the Social Sciences (SPSS) version 20.0 (Chicago, United States of America). and presented in tables. Chi-square was used to test for statistical significance between the tumor location and stage of the disease.

Ethical consideration

Ethical approval to conduct the study was granted by the Ethics and Research Committee of the hospital before the commencement of the study. Confidentiality was maintained, as data gotten from patient's folder and surgical notes were restricted to the researchers.

  Results Top

A total of 59,810 patients with cancers were seen in surgical and radiotherapy and oncology department during the study period (January 2006–December 2015). Of these, 122 cases were colorectal cancer cases accounting for 0.2% of all cases.

Sociodemographic data

The age of presentation ranged from 12 to 78 years. Peak distribution was from 31 to 40 years. The median age was 41 years, mean 42.4 years, and the modal age was 40 years, with a standard deviation ±14.9. The male-to-female ratio was 1.3:1. Civil servants (36%) and those living in the urban region (91%) were the most affected [Table 1].
Table 1: The sociodemographic characteristics of patients

Click here to view

Clinical Presentation

Majority of the patients presented with more than one symptom, bleeding per rectum was the most common complain (n=82) with duration of symptoms ranging from 7-12 months (n=38) [Table 2].
Table 2: Distribution of clinical presentations and duration of symptoms

Click here to view

Anatomical sites, histological patterns, and tumor stage

Multiple sites of origin were noted, with the rectal site being the most common, while the left-sided lesion was more common than the right sided, with a ratio of 1.2:1. The right-sided lesion was more common among the males, with a male-to-female ratio of 1.3:1 [Table 3]. Adenocarcinoma was the most common histological type [Table 4]. Of the n=22 patients with Dukes' stage D disease, n=18 cases were located in the rectum [Table 5].
Table 3: Cross-tabulation of site and patient's sex

Click here to view
Table 4: Histological type, grade, and stage

Click here to view
Table 5: Cross-tabulation of tumor site and stage of the disease

Click here to view

  Discussion Top

The data of 122 patients with colorectal cancers over a 10 year period were collated and analyzed. The study showed an average annual incidence of 12.2 cases/annum. The low annual incidence of 12.2 cases/annum is similar to the low average annual hospital incidence for colorectal cancer (5 cases/annum) reported by Mbah in northwestern part of Nigeria,[12] 6 cases/annum reported by Yawe et al. in northeastern part of Nigeria,[16] and 3.7 cases/year in Burundi.[17] This is in contrast to a study in Southwest of Nigeria with an average of 24 cases/annum [18] and 32.3 cases/annum,[19] in the Republic of Korea with annual incidence as high as 45/100,000,[20] 42.7/100,000 in Slovakia,[20] and 35.2/100,000 in Canada.[20] The low annual incidence in northern Nigeria as compared to southern Nigeria can be attributed to culture, diet, and terrain which are drastically different.[7]

The study revealed that males were more affected than females by a ratio of 1.3:1 which is similar to the study by Abdulkareem et al. in Lagos and Sagamu, Southwest Nigeria,[19] in Jos Northcentral Nigeria with a male-to-female ratio of 1.5:1,[21] and Popoola et al. in Lagos, Southwest Nigeria with a male-to-female ratio of 1.3:1.[22] In Kashmir Valley, India, the male-to-female ratio was 1.2:1.[23] This is in contrast to a study by Madubogwu with a male-to-female ratio of 1:2,[19] with females being more affected than males and Mbah who found an equal ratio of male-to-female ratio of 1:1.[12] The median age in this study was 41 years which is similar to a study done in Jos located in Northcentral Nigeria with the average age of 43.7 years, while the median age was 42 years,[21] Mbah in Sokoto, Nigeria, reported a modal age of fifth decade.[12] Of the 122 cases, 59 patients (48.4%) were 40 years and below, while 63 (51.6%) were 40 years and above. This is comparable to a study in Egypt where 25% of cancers occurred in patients aged <40 years.[24]

From the study, the peak age was 31–40 years which is similar to the findings in Northeast of Nigeria with a peak age in the third decade of life.[25] The youngest patient was 12 years old, while the oldest patient was 78 years old. In Burundi, the mean age was 50.8 years, extremes of 19 years and 78 years.[17] This is in contrast to the US where the peak age is between 65 and 79 years, making it a disease of the elderly and not the young.[26]

The major ethnic groups seen were the Hausas (39.3%). This reflects the geographical region which is predominantly a Hausa settlement but made up of other minority ethnic groups. Majority (91%) were residents of urban settlement and mainly Civil/Public servants (36.0%)by profession, while 9% were residents of rural region and predominantly farmers (5.7%). In contrast to Yawe et al., in North-Eastern Nigeria, it was most common among farmers (29.7%).[16] In Tanzania, East Africa, majority of the patients (70.5%) where from rural areas.[27] In this study, the high incidence in urban region is most likely due to sedentary lifestyle, physical inactivity, excess body weight, and central deposition of adiposity which are established risk factors and probably play a prominent role in the pathogenesis of the disease in our population.[28] Westernization of the diet with resultant overconsumption of energy and developing insulin resistance may contribute to the prevalence in the more affluent region of the country's population, while the lack of specific macronutrients and certain other dietary ingredients in meals may play a part in the underprivileged strata.[28]

The duration of symptoms ranged from 3 weeks to 4 years. with majority of cases (31.1%) presenting between 7-12 Months after first symptoms. This is similar to the findings in Sudan where the median duration until the presentation was 10 months.[29] Similarly, in a study in northeastern Nigeria, the mean duration of symptoms was 14.5 months,[16] in Burundi, the median duration was 20 months from the beginning of symptoms and the first medical visit.[17] Most of the patients presented with more than one symptom. In this study, the most common symptom seen was bleeding per rectum which accounted for 20% (n = 82), weight loss accounted for 14% (n = 58), and change in the bowel 12.7% (n = 52). Similar to the findings by Phillipo et al. where the most common presentation was rectal bleeding 54.2%, change in bowel habit was 51.8%, abdominal pain: 46.1%, constipation: 42.2%, and weight loss: 36.7%,[27] and the findings by Bakari et al. showed that the major clinical features were gastrointestinal tract bleeding (70.3%), change in bowel habits, abdominal pain, weight loss, anorexia, anemia, and rectal mass.[16] This is a reflection of the most common site being the rectum, late presentation, and advanced stage.

The late presentation and advanced disease may be accounted for by poverty, ignorance, and gullibility which lead to unfavorable health-seeking behavior.[18] In this part of the world, rectal bleeding falls under the umbrella of “jedi-jedi”. Jedi-jedi is a spectrum of diseases such as diarrhea, dysentery, low back pain, hemorrhoids, and pruritus ani. “Agbo jedi which is the native brew for this ailment is popular and is sold widely. Patients always vouch for its efficacy until the tumor dictates differently by causing pain, incontinence, or large bowel obstruction.[18] Lack of purchasing power keeps orthodox health care out of the reach of many of these patients. Religious beliefs influence the health-seeking behavior of patients with serious illness, many patients seek healing both in church and through traditional medicine.[18] In fact, in this subregion, it is the general belief that cancer also known as “jeji” was cured only by the native doctor who was the first point of call. Patients were not referred until the disease was advanced.[16]

In this study, the site of tumor was broadly classified into right colonic cancer (cecum, ascending colon, hepatic flexure, and the transverse colon), left colonic cancer (splenic flexure descending and sigmoid colon), and rectal cancer (recto-sigmoid and rectum). The most common tumors were rectal tumors (n = 92) with the rectum accounting for 63% and the left-sided lesion (20%) was more common than the right-sided lesion accounting for 17%, with the right-sided cancers being commoner among males than females. This is similar to the findings by Abdulkareem et al. found in Southwest Nigeria where the left-sided (distal colon) tumor was more common (62%) than right sided (proximal) (14%) ones,[19] and Ahmed et al. in Egypt found that the left-sided tumors were more common at 43%, the right at 36%, and the rectum at 21%.[24] In Tanzania, there were 60.8% of the left sided (distal colon), 23.5% of right-sided (proximal) tumors, and 15.7% of rectal tumors.[27] In contrast with the US where the proximal colon was the most common site (42%), followed by the rectum (28%) and distal colon (23%).[26]

Adenocarcinoma was the predominant histology seen in 73% (n = 89), followed by a variant of adenocarcinoma- mucinous adenocarcinoma was seen in 18% (n = 22), and then, signet ring carcinoma accounted for 2.6% (n = 3). The histological type of adenocarcinoma with neuroendocrine features was seen in the youngest patient age 12 years. In Egypt, histology revealed adenocarcinoma as the most common (91%), two signet ring cell carcinoma (4%), two mucoid carcinoma (4%), and one anaplastic carcinoma (2%).[24] This finding is in agreement with Phillipo et al. in Tanzania who reported similar histological patterns.[27] The histological patterns of mucinous adenocarcinoma and signet ring carcinoma, which were seen in the younger age group <40 years, are usually aggressive/unfavorable behavior and this translates into poor prognosis.[17] Mucinous adenocarcinomas respond poorly to chemotherapy and tend to be located in the proximal colon and associated with microsatellite instability.[27]

About 30% of the cancers were well differentiated, 29.5% were moderately differentiated, 28.7% were not specified, and 11.5% were poorly differentiated. This concurs with the study by Abdulkareem et al. in Southwest Nigeria where the majority were well to moderately differentiated adenocarcinoma (76.4%), mucinous carcinoma (10.7%), and signet ring carcinoma (1.2%) and more common in patients under 40 years compared to well differentiated tumors.[19] Majority of the patients were not staged (59%), of the 41% that were staged, 18% (n = 22) had distant metastasis, 12.3% (n = 15) comprised Dukes' C, 9.0% (n = 11) comprised Dukes' B, and 1.6% (n = 2) were Dukes' A. Most of the patients presented with advanced disease as shown by the stage – Dukes' D and Dukes C (Astler coller C1 and C2). This concurs with Nwafo et al. in Southeast Nigeria where most patients were classified as Dukes' C (33.3%), 30.6% had distant metastasis, 19.9% had stage A, and 16.7% had stage B.[30] Similar findings were found in Yawe et al.'s study in Maiduguri [16] and Popoola et al. in Lagos,[22] all in Nigeria where the patients presented with advanced disease. The findings are comparable with Saidi et al. in Nairobi, Kenya, where most of the patient's presented with Dukes stage C and D [31] and Humadi et al. in Iraq were Dukes C accounted for 71.3%, Dukes' D lesion: 56.9%, and Dukes' B and Dukes'A 7%.[32] Similar findings were found in Zambia by Zahir et al. where 74% of cases presented with stage 3 and 4 diseases.[28] Laishram et al. in Manipur, India, showed that 38.88% of lesions were stage C and above, i.e., involvement of local lymph nodes and distant metastasis.[33] Of the 22 patients with advanced-stage disease (Dukes D), 18 of these were located within the rectum and the test of association between the two variables were not statistically significant.

Late presentation and advanced stage is usually associated with an unfavorable prognosis which may be due to the fact that colorectal cancer has a biologically more aggressive course in Africa and this contributes to the unfavorable staging at the time of presentation and this is further worsened by the combination of ignorance and high cost of medical care.[21] The late presentation can also be attributed to the absence of specific screening measures for colorectal cancer among Nigerians.

  Conclusion Top

The study established that colorectal cancer is becoming more common among the younger age group. The demographics and clinicopathological pattern is similar to other regions within Nigeria and other African countries. These include a slight male preponderance, mostly urban dwellers and civil/public servants. Bleeding per rectum being the most common complaint, rectal predominance and majority of the cases presented at an advanced stage.

The increasing incidence in the young necessitates family screening for genetic mutations since genetic factors may play an important role in the development of this disease. Early detection through public health education, screening programs, affordable and effective treatment, and follow up will help reverse this trend.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

  References Top

Todosi AM, Gavrilescu MM, Scripcariu V. Therapeutic management of colon cancer. J Surg 2014;10:193-6.  Back to cited text no. 1
Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68:394-424.  Back to cited text no. 2
Haggar FA, Boushey RP. Colorectal cancer epidemiology: Incidence, mortality, survival, and risk factors. Clin Colon Rectal Surg 2009;22:191-7.  Back to cited text no. 3
Irabor DO. Colorectal carcinoma: Why is there a lower incidence in Nigerians when compared to Caucasians? J Cancer Epidemiol 2011;2011:675154.  Back to cited text no. 4
Agyemang-Yeboah F, Yorke J, Obirikorang C, Batu EN, Acheampong E, Frempong EA, et al. Patterns and presentations of colorectal cancer at Komfo-Anokye teaching hospital Kumasi, Ghana. Pan Afr Med J 2017;28:121.  Back to cited text no. 5
Madubogwu CI. Colorectal cancer: late presentation and outcome of treatment. Afri medic J 2012;3:13-15.  Back to cited text no. 6
David OI. Ethnic differences in colon and rectal cancer incidence in Nigeria: A case of Dietary determinants? Ann Niger Med 2012;6, issue: 2, page :71-74  Back to cited text no. 7
Siegal R, Jamal A. American Cancer Society. Colorectal cancer: facts and figure 2011, figure 2012, figure 2013. Atlanta: American Cancer Society, 2011.  Back to cited text no. 8
Sack J, Rothman JM. Colorectal cancer: Natural history and management. Hosp Phys 2000;36:64-73.  Back to cited text no. 9
Omranipour R, Doroudian R, Mahmoodzadeh H. Anatomical distribution of colorectal carcinoma in Iran: A retrospective 15 year study to evaluate rightward shift, Asian pacific J cancer prev. 2012; 13:279-82.  Back to cited text no. 10
Halperin EC, Perez CA, Brady LW. Perez Brady's Principles and Practice of Radiation Oncology: 6th Ed. Lippincott Williams and Wilkins 2008., Wolters Kluwer, Philadelphia, Pennsylvania. 2013.  Back to cited text no. 11
Mbah N. Hospital frequency of large bowel cancer: Factors thought to influence outcome. Niger J Clin Pract 2009;12:37-41.  Back to cited text no. 12
Tárraga López PJ, Albero JS, Rodríguez-Montes JA. Primary and secondary prevention of colorectal cancer. Clin Med Insights Gastroenterol 2014;7:33-46.  Back to cited text no. 13
Hadjipetrou A, Anyfantakis D, Galanakis CG, Kastanakis M, Kastanakis S. Colorectal cancer, screening and primary care: A mini literature review. World J Gastroenterol 2017;23:6049-58.  Back to cited text no. 14
Knapp GC, Alatise OI, Olasehinde OO, Adeyeye A, Ayandipo OO, Weiser MR, et al. Is colorectal cancer screening appropriate in Nigeria? J Glob Oncol 2019;5:1-0.  Back to cited text no. 15
Yawe K T, Bakari A A, Pindiga U H, Mayun A A. Clinicopathological pattern and challenges in the management of colorectal cancer in Sub-Saharan Africa. J Chinese Clinl Med. 2007;2:688-694.  Back to cited text no. 16
Renovat N, Richard K, Gabriel N, Sylvan N. Colorectal cancer epidemiological, clinical and histopathological aspects in Burundi. Open J Gastroenterol 2016;6:83-7.  Back to cited text no. 17
David OI, Oludapo OA, Omobolaji OA. The present status of the management of colon and rectal cancer in Nigeria. J Cancer Res 2014;2014:267190.  Back to cited text no. 18
Abdulkareem F B, Abudu E K, Awolola N A, Elesha SO, Rotimi O, Akinde OR et al. Colorectal carcinoma in Lagos and Sagamu, Southwest Nigeria: A histological review. World Journal of gastroenterology 2008, November 14;14:6531-5.  Back to cited text no. 19
Ferlay J, Soerjomataram I, Ervik M, Eser M, Dikshit R, Eser S, Mathers C, et al. GLOBOCAN 2012 v1.1, Cancer Incidence and Mortality Worldwide. IARC Cancer Base No. 11. Lyon, France: International Agency for Research on Cancer; 2014. Available from: http://globocan.iarc.fr. [Last accessed on 2015 Jan 16].  Back to cited text no. 20
Ohayi SA, Nzegwu MA, Silas AA, Mandong BM. Histopathological pattern of colorectal tumours in Jos university Teaching Hospital (JUTH), Jos. A 5 year retrospective review from (January 1999- December 2003). Adv Biores 2011;2:127-31.  Back to cited text no. 21
Popoola A, Ibrahim N, Omodele F, Igwilo I, Soyemi S. Clinicopathological presentation of colorectal cancer seen in Lagos State University Teaching Hospital. Maced J Med Sci 2012;5:411-5.  Back to cited text no. 22
Javid G, Zargar SA, Rather S, Khan AR, Khan BA, Yattoo GN, et al. Incidence of colorectal cancer in Kashmir valley, India. Indian J Gastroenterol 2011;30:7-11.  Back to cited text no. 23
Ahmed G, Basel E, Aida A, Anthony A. Colorectal cancer in Egypt is commoner in young people: Is this cause for alarm? Alexandria J Med 2014;50:197-201.  Back to cited text no. 24
Abubakar AB, Haruna N, Abubakar SA, Gali M, Usman BD. Presentations and management of colorectal cancer in under 40 years of AGE in the sub-Saharan Africa: A multi-centre study. Sch J Appl Med Sci 2014;2:3284-9.  Back to cited text no. 25
Siegel R, Desantis C, Jemal A. Colorectal cancer statistics. 2014. CA Cancer J Clin 2014; 64:104-17.  Back to cited text no. 26
Phillipo LC, Mabula DM, Joseph BM, Peter FR. Clinicopathological pattern and challenges of management of colorectal cancer in a resource limited setting: A Tanzanian experience. World J Surg Oncol 2013;11:88.  Back to cited text no. 27
Zahir MN, Azhar EM, Rafiq S, Ghias K, Shabbir-Moosajee M. Clinical features and outcome of sporadic colorectal carcinoma in young patients: A cross-sectional analysis from a developing country. ISRN Oncol 2014;2014:461570.  Back to cited text no. 28
Mutaz MM, Amagid MM, Elsaggad, Mutaaz AE. Colorectal cancer in Sudanese patients. Int J Med 2015;3:98-102.  Back to cited text no. 29
Nwafo DC, Ojukwu JO. Malignant disease of the colon, rectum, and anus in Nigerian Igbos. Ann R Coll Surg Engl 1980;62:133-5.  Back to cited text no. 30
Saidi HS, Karuri D, Nyaim EO. Correlation of clinical data, anatomical site and disease stage in colorectal cancer. East Afr Med J 2008;85:259-62.  Back to cited text no. 31
Al-Humadi AH. Epidemiology of colon and rectal cancer in Iraq. World J Colorectal Surg 2008;1:15.  Back to cited text no. 32
Laishram RS, Nisa K, Shimray R, Devi BS, Punyabati P, Sharma CD. Histopathological evaluation of colorectal carcinomas status in Manipur, India. Int J Pathol 2010;8:5-8.  Back to cited text no. 33


  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5]


Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

  In this article
Materials and Me...
Article Tables

 Article Access Statistics
    PDF Downloaded7    
    Comments [Add]    

Recommend this journal