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Annals of African Medicine
Annals of African Medicine Society
ISSN: 1596-3519
Vol. 5, Num. 3, 2006, pp. 118-121

Annals of African Medicine, Vol. 5, No. 3, 2006, pp. 118-121

Non-Squamous Cell Carcinoma of the Cervix in Zaria, Northern Nigeria:  A Clinico-Pathological Analysis

1M. A. Abdul, 2A. Mohammed, 2A. Mayun and 1S. O. Shittu

Departments of 1Obstetrics and Gynaecology, and 2Morbid Anatomy, Ahmadu Bello University Teaching Hospital, Zaria, Nigeria
Reprint requests to: Dr. M.A. Abdul, Department of Obstetrics and Gynaecology, Ahmadu Bello University Teaching Hospital Zaria, Nigeria. E-mail: Maabdul90@yahoo.com

Code Number: am06028

Abstract

Background: The incidence of Adenocarcinoma of the cervix is on the increase in many parts of the world. There is paucity of information regarding non-squamous cancer of the cervix in our setting.
Method:Descriptive analysis involving consecutive histological confirmed cases of non-squamous malignancy of the cervix over a ten-year period from January 1994 to December 2003.
Results: During the period of study, there were 361 histological confirmed cases of cervical cancer of which 322 (89.2%) were squamous cell carcinoma and 10.8% were non-squamous cell malignancy. All the 39 cases of non-squamous cell cancer except one were adenocarcinoma (97.4%). The exception was a case of leiomyosarcoma. Pure adenocarcinoma is the commonest form of adenocarcinoma (60.5%) followed by adenosquamous variant (21.1%). The mean age of the 39 patients was 42.9±7.2years (range 29 – 75 years) and mean parity of 5.5±2.9 (range 2 – 12). All the patients were symptomatic with abnormal uterine bleeding associated with vaginal discharge seen in 89.5% of cases. 80% of the patients were diagnosed in advanced stage.
Conclusion: Non-squamous cancer of the cervix constitutes 11% of all cervical malignancy in Zaria and adenocarcinoma is the commonest form. The clinical profile of adenocarcinoma of the cervix does not appear to differ from that of squamous cell cancer. Further studies are needed to compare the prognosis between the two histological cell types in our environment.    

Key words: Cervix, carcinoma, non-squamous

Résumé

Introduction : La fréquence des cas d’adénocarcinome de col est en augmentation dans bien des parties du monde.  Il y a une pénurie d’information en ce qui concerne cancer non squameux du col dans notre milieu.
Méthodes :Une analyse descriptive impliquant des cas maligns non squameux histologiquement confirmés de col au cours d’une période de dix ans à partir du janvier 1994 au décembre 2003.
Résultat :Pendant la période d’étude, il y avait 361 cas des cancers cervicaux histologiquement confirmés dont 322 soit 89,2% étaient cellulite carcinome squameuse et 10,8% étaient cellulite carcinome squameuse et 10,8% étaient cellulite malignité non-squameuse.  Tous les 39 cas du cancer de cellule non-squameux à l’exception d’un cas étaient adénocarcinome (97,4%).  L’exception était un cas de léiomyosarcome.  Adénocarcinome pur est une forme la plus ordinaire d’adénome carcinome 60,5% suivi par adénosquame variant (21,1%).  L’âge moyen de 39 patients était 42,9+-7,2 ans (tranche 2 – 12).  Tous les patients étaient symptomatiques avec l’utérin saignant anormal associé au écoulement/pertes vaginales vues chez 89,5 des cas.  80% des patients ont été diagnostiqués étape en avance.
Conclusion : Cancer de col non-squameux constitue 11% de tous les cas des maligns cervicaux à Zaria et adénocarcinome est la forme la plus ordinaire.  Le profil clinique d’adénocarcinome du col ne semble pas être différant de celui du cancer de la cellule squameuse.  Des études supplémentaires sont exigées afin de comparer le prognose entre les deux types des cellules histologiques dans notre milieu.

Mot clés :Col, carcinome, non-squameux

Introduction

Cervical cancer is a major public health problem in many developing countries, due largely due to limited access to screening and treatment.1, 2 Of the 400,000 new cases of cervical malignancy occurring annually worldwide, >80% occur in developing countries, 200,000 of whom die of the disease.2, 3

In Sub-Saharan Africa, carcinoma of the cervix is the commonest genital tract malignancy encountered, accounting for over 50% of cases. 4-7 Cancer of the cervix and breast, are the leading causes of cancer-related death among women in Africa.8, 9

Squamous cell carcinoma is the commonest histological cell-type encountered accounting for over 85% of variants followed by adenocarcinoma. 10, 11 The incidence of adenocarcinoma has been on the increase partly due to increasing incidence of Human Papilloma Virus (HPV) infection and also due to increased detection of preinvasive and early invasive squamous cell carcinoma leading to a shift in histologic pattern in favour of adenocarcinoma.10, 12-18 Whether this trend is applicable to Sub-Saharan Africa is not clear as effective population-based screening is not widely available.

Most of the available reports that have characterised the pattern of cervical cancer in this environment have either focused on all cell types or the predominant squamous cell variant. Few reports have been directed at the less radiosensitive non-squamous cell types.  

Materials and Method

Consecutive histologically confirmed cases of cancer of the cervix from January 1994 – December 2003 were retrieved from the cancer register of the department of pathology, Ahmadu Bello University Teaching Hospital, Zaria, Nigeria. Cases of adenocarcinoma of the cervix and other non-squamous cell cancer were selected and case notes analysed.  The clinical profile and histological pattern of   these   cases   were   studied   including   those  of squamous cell carcinoma. Data was analysed using SPSS version 10.0.

Results

During the study period, there were 361 histologically confirmed cases of cervical malignancy of which 322 (89.2%) were squamous cell carcinoma and 10.8% were non-squamous cell cancer. Of the 39 non-squamous cell cases, 38 (97.4%) were adenocarcinomas and only one case of leiomyosarcoma. The histological variants of the 38 adenocarcinoma cases are shown in table 1. The mean age of the 39 patients with non-squamous cell carcinoma was 42.9 ± 7.2years (range 29-75) and mean parity of 5.5 ± 2.9 (range 2 – 12).  All the 39 patients were symptomatic, with abnormal uterine bleeding associated with vaginal discharge seen in 89.5% of cases. Four cases presented with post coital bleeding associated with gross lesion on the cervix.  The macroscopic features and Federation of International Gynecology and Obstetrics (FIGO) staging of the non-squamous cell cancers encountered is shown in tables 2; stage IB 3 (7.7%), IIA 5 (12.8), IIB 9 (23.1) and III 22 (56.4).  The cervical polyp was the only case of leiomyosarcoma encountered in the study. Squamous and non-squamous malignancies of the cervix are compared in table 3.

Table 1:  Histologic pattern of adenocarcinoma in 38 patients

Histological type

No. (%)

Pure adenocarcinoma

23 (60.5)

Adenosquamous carcinoma

8 (21.1)

Mucinous adenocarcinoma

1 (2.6)

Mesonephroid adenocarcinoma

1 (2.6)

Papillary adenocarcinoma

1 (2.6)

Carcinoid tumour

1 (2.6)

Clear cell adenocarcinoma

1 (2.6)

Poorly differentiated adenocarcinoma 

2 (5.3)

Total

38 (100)

Table 2: Summary of gross features and histologic type of non-squamous cell carcinoma of the cervix

Histologic type

Gross feature

Exophytic growth

Endophytic growth

Ulcerative lesion

Polyploid mass

Pure adenocarcinoma

16

5

2

-

Adenosquamous

7

-

1

-

Mucinous adenocarcinoma

1

-

-

-

Mesonephroid adenocarcinoma

1

-

-

-

Papillary adenocarcinoma

1

-

-

-

Carcinoid tumour

-

1

-

-

Clear cell adenocarcinoma

1

-

-

-

Poorly differentiated adenocarcinoma

2

-

-

-

Leiomyosarcoma

-

-

-

1

Total (%)

29(74.3)

6(15.4)

3(7.7)

1(2.6)

Table 3: Comparison of clinico-pathological features of squamous and non-squamous malignancies of the cervix

Factor

Non-squamous cell tumour (n=39)

Squamous cell carcinoma (n=322)

p value

Mean age

42.9± 7.2 yrs

43.1± 8.2 yrs

NS

Mean parity

5.5 ± 2.9 yrs

5.9 ± 3.1

NS

Predominant symptom

Abnormal uterine bleeding with vaginal discharge

Abnormal uterine bleeding with vaginal discharge

-

Predominant gross pathological feature

Exophitic growth in 74% of cases

Exophitic growth in 76% of cases

NS

FIGO staging

80% with advance disease

76% with advance disease

NS

Commonest histologic type

Pure adenocarcinoma

Large-cell non keratinising

-

NS: not significant; FIGO: Federation of International Gynecology and Obstetrics

Discussion

The mode of clinical presentation and staging in the present report do not differ from established data concerning cancer of the cervix in Africa. 19-24  In this study, mean age at presentation was 43 years, abnormal uterine bleeding with vaginal discharge were present in 90% of cases and 80% were diagnosed with advance disease (≥stage II B). These characteristics were similar with that of squamous cell carcinoma (table IV). Thus it appears that in terms of mode of presentation and staging, non-squamous cell cancer (adenocarcinoma) do not differ from squamous cell carcinoma in our setting.  Non-squamous cell carcinoma accounts for 10-22% of all cervical cancers while squamous cell type accounts for the remainder (80-90%). Our figure of 11% for non-squamous cell carcinoma confirmed earlier reports.10-11, 25  

In this study, adenocarcinoma is the predominant tumour type (97%) for non-squamous cancers, and 61% of adenocarcinomas were well differentiated (pure) adenocarcinomas followed by adenosquamous variant (21%).  Others such as papillary serous and clear cell carcinoma were not common.  This is in conformity with established knowledge.10, 11 Only one case of sarcoma of the cervix was encountered in this study. Lymphomas, melanomas or basal cell carcinoma were not seen among our patients.  It can be concluded that adenocarcinoma is the prototype of non-squamous cell malignancy of the cervix and the clinical profile (presentation and staging) of patients with cervical adenocarcinoma do not appear to differ from that of squamous cell cancer in our setting. Further studies are needed to compare the prognosis between the two histological cell types in our environment.

References

  1. Kitchener HC. Recent developments in cervical cancer. Africa Health 1999; 21: 24-26
  2. Sherris J. Preventing cervical cancer in low-resource settings.  Outlook 1998; 16: 1-8
  3. Kitchener HC, Symonds P. Detection of cervical intraepithelial neoplasia in developing countries.  Lancet 1999; 353: 856-857
  4. Nkyekyer K. Pattern of gynaecological cancers in Ghana. East AFr Med J 2000; 77: 534-538
  5. Galadanchi HS, Jido TA, Muhammed AZ, Uzoho CC, Uchicha O. Gynaecological malignancies at Aminu Kano Teaching Hospital Kano, Nigeria: a five year review.  Tropical Journal of Obstetetrics and Gynaecology 2002: 19 (Suppl 2): 10
  6. Gichangi P, Estambule B, Bwayo J, Rogo K, Ojwang S, Opiyo A, Temmerman M. Knowledge and practice about cervical cancer and Pap smear testing among patients at Kenyatta National Hospital, Nairobi, Kenya.  Int J Gynecol Cancer 2003; 13: 827-833
  7. Petry K U, Scholz U, Hollwitz B, Von Wasielewski R, Meijer CJ. Human papilloma virus coinfection with Shistosoma hematobium and cervical neoplasia in rural Tanzania.  Int J Gynecol Cancer 2003; 13: 505-509
  8. Ajayi IO, Adewole IF. Breast and cervical cancer screening activities among family physicians in Nigeria. Afr J Med med Sci 2002; 81: 305-309
  9. Amrani M, Lalaoui K, EL Mzibri M, Lazo P, Belabbas MA. Molecular detection of human papillomavirus in 594 uterine cervix samples from Moroccan women. J Clin Virol 2003; 27: 286-295
  10. Disaia P J, CreasMan WT. Clinical gynaecologic oncology. Mosby, St. Louis, 1989; 67-127
  11. Holschneider CH. In: Decherney AH, Nathan L (eds). Current obstetric and gynaecologic diagnosis and treatment. Lange, New York, 2003; 894-914
  12. Lakhtakia R, Singh MK, Taneja P, Kapila K, Kumar S. Villoglandular papillary adeno- carcinoma of the cervix: case report  J Surg Oncol 2000; 74: 297-299
  13. Lee K R, Flynn CE. Early invasive adenocarcinoma of the cervix. Cancer 2000; 89: 1048-1055
  14. Acevedo CM, Henriquez M, Emmert B, Michael R, Chuaqui RF. Loss of heterozygosity on chromosome arms 3p and 6p in microdissected adenocarcinoma of the uterine cervix and adenocarcinoma insitu. Cancer 2002; 94: 793-802 Pekin T, Kavak Z, Yildizhan B, Kaya H. Prognosis and treatment of primary adenocarcinoma and adenosquamous cell carcinoma of the uterine cervix.  Eur J Gynaecol Oncol 2001; 22: 160-163
  15. Recoules – Arche A, Rouzier R, Rey A, et al. Does adenocarcinoma of the uterine cervix have a worse prognosis then squamous cell carcinoma?  Gynecol Obstet Fertil 2004; 32: 116
  16. Berrington de Gonzalez A, Sweetland S, Green J. Comparison of risk factors for squamous cell and adenocarcinoma of the cervix: a meta analysis.  Br J Cancer 2004; 90: 1787-1791
  17. Quinn M A. Adenocarcinoma of the cervix - are there arguments for a different treatment policy? Curr Opin Obstet Gynecol 1997; 9: 21-24
  18. Mati JK, Mbugua S, Ndavi M. Control of cancer of the cervix: feasibility of screening for premaligant lesions in an African environment.  IARC Sci Publ 1984; 63: 451-463
  19. Emembolu JO, Ekwempu CC. Carcinoma of the cervix uteri in Zaria: etiological factors.  Int J Gynaecol Obstet 1988; 26: 265-9.
  20. Kasule J. The pattern of gynaecological malignancy in Zimbabwe.  East Afr Med J 1989; 66: 393-399
  21. Rogo K O, Omany J, Onyango JN, Ojwang SB, Stendahl N. Carcinoma of the cervix in the African setting.  Int J Gynaecol Obstet 1990; 33: 249-255
  22. Briggs ND, Katchy KC. Pattern of primary gynaecological malignancies as seen in a tertiary hospital situated in the Rivers State of Nigeria.  Int J Gynaecol Obstet 1990; 31: 159-161
  23. Adewole IF, Edozien LC, Babarinsa IA, Akang EE. Invasive and insitu carcinoma of the cervix in young Nigeria: a clinico-pathologic study of 27 cases.  Afr J Med Sci 1997; 26: 191-193
  24. Gallup DG, Stock R J, Talledo OE. Current management of non-squamous carcinoma of the cervix. Oncology (Huntingt) 1989; 3: 95-102.

Copyright 2006 - Annals of African Medicine

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