PATTERN OF PROSTRATE DISEASES- A HISTOPATHOLOGICAL STUDY IN JAMMU

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PATTERN OF PROSTRATE DISEASES- A HISTOPATHOLOGICAL STUDY IN JAMMU *Neha Angurana Dayanand Medical College & Hospital, Ludhiana- 141008 Punjab, India *Author for Correspondence ABSTRACT Benign hypertrophic prostate (BHP) is the most common urologic disorder in men beyond 40 years of age group and is almost present in men aged 80-90 years of age group. There are many similarities between BHP and. Most s arise in prostate together with BHP and is found accidentally in 10% of TRUP specimens. BHP is not premalignant lesion of the prostatic but it may be related to prostate arising in transition zone. As there is no study from Jammu region so we have conducted this study to survey pattern of prostate diseases based on analysis of histopathological specimens. The data will be useful for planning facilitied after management of prostatic diseases especially prostate. The present study was conducted to determine histologic pattern and age distribution of various prostatic lesions by analyzing prostate specimens and to carry out detaied morphologic study of various prostatic lesions along with grading and scoring of carcinomas according to the Gleason system. Out of 200 prostate specimens, majority of the cases were of BHP alone 50.5% (101/200). The decade wise distribution of various prostate lesions, the incidence of BHP alone and BHP with prostatitis was highest in 61-70 year. The age range noted in BHP was from 52-90 years. A similar increasing trend was seen in age incidence and distribution of prostate which was highest in the 61-70 year age group. Thus, the commonest prostatic lesion encountered was BHP, the incidence of prostate being low. BHP was observed in 51-80 year age group with peak in the 7 th decade. The morphologic pattern of BHP consisted predominantly of fibroglandular hyperplasia, followed by squamous metaplasia other variants include clear cell hyperplasia, stromal hyperplasia, transitional hyperplasia and basal cell hyperplasia. Keywords: Prostrate Diseases, Benign Hypertrophic Prostate INTRODUCTION Benign hypertrophic prostate (BHP) is the most common urologic disorder in men beyond 40 years of age group and is almost present in men aged 80-90 years of age group. The clinical incidence of this disease is only 8% during the 4 th decade, but it reaches 50% in the 5 th decade and 75%in the 8 th decade (Rosai, 2005). Advanced age and an intact androgen supply are the only undisputed risk factors for BHP (Bostwick et al., 1992). There are many similarities between BHP and (Bostwick and Amin, 1997). Most s arise in prostate together with BHP and is found accidentally in 10% of TRUP specimens. BHP is not premalignant lesion of the prostatic but it may be related to prostate arising in transition zone (Difenbach et al., 2002). In Europe and United States, prostate is the most commonly diagnosed malignancy in elderly men and second leading cause of related deaths in the male population (Ro et al., 2001). In 1993, the Gleason grading system was recommended by WHO consensus conference (Murphy et al., 1993). This system is based on glandular architecture and is an effective prognostic factor on all prostatic samples (Egevad et al., 2004). As there is no study from Jammu region so we have conducted this study to survey pattern of prostate diseases based on analysis of histopathological specimens. The data will be useful for planning facilitated after management of prostatic diseases especially prostate. Aim and Objectives The present study was conducted to determine histological pattern and age distribution of various prostatic lesions by analyzing prostate specimens and to carry out detailed morphologic study of various prostatic lesions along with grading and scoring of carcinomas according to the Gleason system. Copyright 2014 Centre for Info Bio Technology (CIBTech) 163

MATERIALS AND METHODS The study was approved by the Institute Ethical Committee and was conducted retrospectively as well prospectively. Retrospective study comprising of collection of cases of prostatic specimens for a period of four years. All the available slides were retrieved and reviewed. Prospective study comprising of fresh cases of prostrate lesions that were present in the course of one year. During this period, a total of 200 prostate specimens were received. In each case brief clinical history and physical examination along with other clinical information provided in requisition form regarding age, sex, type of prostatic biopsy and clinical diagnosis is taken into consideration and recorded in a pre-structured performa after obtaining their written consent. All the specimens were fixed in 10% neutral buffered formalin immediately. Three types of prostrate tissue biopsy were received-open prostatectomy, TURP chips and trucut needle biopsy. Tissue processing was done in automatic tissue processor (Histokinette), followed by staining done by Haematoxylin and Eosin (Stevens, 1986). The slides were examined under light microscope and observations were made. RESULTS AND DISCUSSION Results The data was recorded and compiled. All prostatic lesions were categorized into benign and malignant and among benign lesions pattern of prostatic hyperplasia and inflammatory disorders were tabulated with their frequency and age distribution (Table 1). Out of 200 prostate specimens, majority of the cases were of BHP alone 50.5% (101/200). The decade wise distribution of various prostate lesions, the incidence of BHP alone and BHP with prostatitis was highest in 61-70 year. The age range noted in BHP was from 52-90 years. A similar increasing trend was seen in age incidence and distribution of prostate which was highest in the 61-70 year age group. In majority of the BHP cases, varying portions of glandular and stromal proliferative tissue was seen. These cases were diagnosed as fibroglandular hyperplasia which constituted 78.5% (146/186) of total BHP cases. The next common variant was BHP with squamous metaplasia 11.8% (22/186). Clear cell cribriform hyperplasia and stromal hyperplasia constituted 3.8% (7/186) and 2.7% (22/186) cases respectively. BHP with transitional cell hyperplasia and basal call hyperplasia were the least common variants (Figure 1) where as all cases of prostatic was adenocarcinoma. Out of 14 cases of prostate carcinoma, 33.7% (5/14) were graded in Gleason score 4-6 while 64.3% (9/14) were Gleason score 7-10 (Figure 2). Discussion Prostatic tissue is a common specimen received for histopathological examination. With the increasing longevity and ageing population, the pathology of the prostate may claim a separate domain of its own. Prostatism is a common malady in the geriatric age group. BHP and carcinoma of the prostate are increasingly frequent with advancing age. Table 1: Distribution of Various Prostate Lesions and their demographic profile Diagnosis No.Of cases Percentage Age distribution(in years) (%) 51-60 61-70 71-80 81-90 BHP alone 101 50.5 28 44 23 06 BHP+ Prostatis 85 42.5 23 43 11 08 Prostate alone BHP+Prostate PIN+Prostate 10 5 02 04 02 02 02 1 00 01 01 00 02 1 00 02 00 00 Copyright 2014 Centre for Info Bio Technology (CIBTech) 164

Figure 1: Variants of BHP Figure 2: Gleason Score Of Prostate Cancer (n=14) There are various lesions which have increased the burden of the patient suffering from these diseases. The role of the pathologist in assessing them has assumed much importance with the advent of needle biopsy. In our study, the predominant lesion was BHP (50.5%) followed by BHP with prostatitis (42.5%) and prostate (7%). This pattern is comparable to that of other studies done by Jayaram et al., (1993) Shakya et al., (2003) Rekhi et al., (2004) Anim et al.,(1998) found mean age of 63 years while Di Silverio et al., (2003) found mean age of 68.85. Our study is in close match with the studies of Anim et Copyright 2014 Centre for Info Bio Technology (CIBTech) 165

al., (1998) and Di Silverio et al., (2003) in relation to the mean age in years for BHP. Our study was in agreement with Mittal et al., (1989) Ibrahim (2003), Karkuzhali et al., (2004) in respect that fibroglandular hyperplasia was most commonly noted. However there are higher no of cases of BHP with basal cell hyperplasia, clear cell cribriform hyperplasia and stromal hyperplasia in studies of Mittal et al., (1989) and Karkuzhali et al., (2004) Squamous metaplasia is the next predominant morphological feature of BHP, attributable to the fact that it is a reactive process that occurs due to hormonal manipulation or when the centre of the nodule undergoes haemorrhagic necrosis. The detection of basal cell carcinoma is attributable to the fact that epithelial hyperplasia which starts with basal cell hyperplasia which follows regeneration of glands (Anim et al., 1998). In present study cases of prostatic carcinoma were 7% (14/200) were adenocarinoma and perineural invasion was observed in 21.43% (3/200), Alberto et al., (2005) found adenocarcinoma prostate in 546/1422 patients with clinical suspicion of prostate an dperineural invasion was seen in 25% (137/1422) cases. In this study, out of 14 cases of prostate, 5 (35.7%) cases were graded in Gleason score 4-6 while 9 (64.3%) cases were graded in Gleason score of 7-10, where as in other studies done by Ahmed and Muzaffar (2002) majority of tumours were moderately differentiated. Other study done by Angwafo et al., (2003) found 6 cases of prostate in needle biopsies performed on 24 cases. Gleason score ranged from 5 to 9. Conclusion Thus, the commonest prostatic lesion encountered was BHP, the incidence of prostate being low. BHP was observed in 51-80 year age group with peak in the 7 th decade. The morphologic pattern of BHP consisted predominantly of fibroglandular hyperplasia; followed by squamous metaplasia other variants include clear cell hyperplasia, stromal hyperplasia, transitional hyperplasia and basal cell hyperplasia. REFERENCES Ahmed Z and Muzaffar S (2002). Prostatic Carcinoma with emphasis on Gleason s grading: an institution based experience, The Journal of the Pakistan Medical Association 52(2) 54-6. Alberto A, Katia R, Marcos F, Alexandre C, Luciano J and Miguel S (2005). Prostate Biopsy: Is age important for determining the pathological features in prostate, International Brazilian Journal of Urology 31(4). Angwafo FF, Zaaher A, Befidi- Mengue R, Wonkam A, Takougang I and Powell I et al., (2003). High Grade intra epithelial neoplasia and prostate in Dibombari, Cameroon, Prostate Cancer and Prostatic Diseases 6 34-8. Anim JT, Ebrahim BH and Sathar SA (1998). Benign disorders of prostate: A histopathological study, Annals of Saudi Medicine 18(1) 22-7. Bostwick DG and Amin MB (1997). Male reproductive system. In: Andersons Pathology, 10 th edition, edited by Damjanov I and Linder J (Mosby) Missouri 2 2197-208. Bostwick DG, Cooner WH and Denis L (1992). The association of benign prostatic hyperplasia and of the prostate, Cancer 70 291. Di Silvero F, gentile V, DeMatteis A, Mariotti G, Giuseppe V and Luigi P et al., (2003). Distribution of inflammation, pre malignant lesions, incidental carcinoma in histologically confirmed benign prostatic hyperplasia: A retrospective analysis, European Urology 43(2) 164-175. Difenbach MA, Dorsey J, Uzzo RG, Hanks GE, Greenberg RE and Horwitz E et al., (2002). Decision making strategies for patients with localized prostate, Seminars in Urologic Oncology 20 52-62. Egevad L, Granfors T, Karlberg L, Bergh A and Stattin P (2004). Prognostic value of Gleason score in prostate, pathology and genetic of the urinary system and male genital organs 167-214. Ibrahim M (2003). Pattern of Prostatic disease in Saudi Arabia, The Internet Journal of Pathology 2(2). Jayaram G, Nakra N, Verma AK and Goel GD (1993). Transrectal fine needle aspiration of prostate, Association of Physicians of India 41(6) 364-6. Karkhuzali P, Bhattacharyya M and Gnanaguruparan A (2004). Histopathologic Spectrum of prostatic lesions in surgical biopsies specimens. Indian Journal of Pathology and Microbiology 47 132-3. Copyright 2014 Centre for Info Bio Technology (CIBTech) 166

Mittal BV, Amin MB, Kinare SG (1989). Spectrum of histological lesions in 185 consective prostatic specimens, Journal of Postgraduate Medicine 35 157. Murphy GP, Busch C, Abrahamsson PA, Epstein JI, McNeal JE and Miller GJ et al., (1993). Histopathology of localized prostate. Consensus conference on diagnosis and prognostic parameters in localized prostate. Stockholm, Sweden, Journal of Urology and Nephrology 162 7-42. Rekhi B, Jaswal TS and Arora B (2004). Premalignant lesions of prostate and their association with nodular hyperplasia and carcinoma prostate. Indian Journal of Cancer 41 60-5. Ro JY, Amin MB, Saihin AA and Ayala AG (2001). Tumors and timorous conditions of the male genital and urinary tract, Diagnostic Histopathology of Tumors 1 773-4. Rosai J (2005). Male reproductive system, In: Rosai and Ackerman s Surgical Pathology, 9 th edition (Mosby) Missouri 1 1361-8. Shakaya G, Malla S and Shakya KN (2003). Salient and co-morbid features in benign prostatic hyperplasia: a histopathological study of prostate, Kathmandu University Medical Journal 1(2) 104-9. Stevens A (1986). The haematoxylins, In: Theory and Practice of Histological Techniques, 2 nd edition, edited by Bancroft JD and Stevens A, Churchill Livingstone, Edinburgh 109-121. Copyright 2014 Centre for Info Bio Technology (CIBTech) 167