Keywords
Hysterectomy, Adenomyosis, Menorrhagia.
Abstract
Adenomyosis is a myometrial lesion which is characterized by the presence of ectopic endometrium within the myometrium
with or without hyperplasia of the surrounding myometrium. The study which was carried out from January 2010 to
December 2011 over a period of 2 years to study the clinical profile of all the patients whose hysterectomy specimens showed
adeno¬myosis. Three hundred and ninety (390) patients were studied. The prevalence of adenomyosis was 24.43%. 86%
of the patients were seen in the age group of 31-50 years. 94.3% of the patients were multiparous. The dominant symptom
was menorrhagia (75.6%), followed by dys¬menorrhoea (33.3%). DUB was clinically suspected in 33.9% of the cases
followed by fibroid (24.6%) and adenomyosis (22.3%). The occurrence of adenomyosis was mostly seen in the age group
of 31-50 years in the present study, which was contrary to that which was observed in some other stud¬ies, which showed
the maximum occurrence after 40 years. The parity and the clinical symptoms correlated with those of other studies.
Introduction
Adenomyosis is a myometrial lesion which is characterized by
the presence of an ectopic endometrium within the myome-
trium with or without hyperplasia of the surrounding myome-
trium. The endometrial tissue should be at least 100x field or
one low power field (about 2.5 mm) deep from the endomy-
ometrial junction The endometrial glands may be inactive or
hormonally responsive. In some cases, the glands are scant
or absent and such cases may be mistaken for low-grade en-
dometrial stromal sarcoma. A majority of the cases are diag-
nosed following the histological examination of hysterectomy
specimens, but the exact prevalence in the ‘normal’ popula-
tion is unknown. The percentage of hysterectomy specimens
which contain adenomyosis varies from 5–70% [1]. This wide
variation may be partly explained by the histological criteria
which is used and/or by the number of tissue blocks which are
examined. The specificity of the pre-operative diagnosis which
is based on the clinical picture is poor, ranging from 2.6–26%
[2]. A majority of the cases are reported in women who are
aged 40–50 years and there is a positive association with the
parity also. The patients with adenomyosis present with men-
orrhagia (40–50%), dysmenorrhoea (10–30%) and metrorrha-
gia (10–12%) and, occasionally, dyspareunia [3, 4, 5].
Material and methods
In the period from January 2010- December 2011, 1596 hys-
terectomy specimens were received and studied at the De-
partment of pathology, GMC Jammu. Adenomyosis was diag-
nosed when the distance from the endo-myometrial junction
to the foci of the adenomyosis was more than one low pow-
er field (Fig. 1). For the study, the paraffin sections of all the
hysterectomy specimens were examined. 390 patients were
diagnosed to be having adenomyosis. The medical records in
which the histopathological report was adenomyosis were re-
viewed and information regarding age, parity, the chief com-
plaints, and the clinical diagnosis was obtained. The data was
entered in simple tables and was analyzed.
Results
Of the 390 patients, 46.9% were in the age group of 41-
50 years, 39.2% were in the age group of 31-40 years and
10.8% were in the age group of 51-60 years. In the extremes
of age, the prevalence decreased to 2.1% in the age group
of 21-30 years and 1.0% were above 60 years of age (Table
1). 94.3% of the patients were multiparous. A majority of
them were of parity 2 and 3. In nulliparous and uniparous
women, the prevalence was 2.6% and 3.1% respectively. In
women with a parity of ≥ 5 also, the prevalence was found
to be decreased (4.3%)(Table 2). The dominant symptom was
menorrhagia (75.6%), followed by dysmenorrhoea (33.3%).
Only 8.9% of the patients had chronic pain in the abdomen.
Adenomyosis was also diagnosed in patients who had com-
plaints of a mass descending per vagina, post-menopausal
bleeding and a mass in the abdomen (Table 3). The pre-opera-
tive clinical diagnosis was dysfunctional uterine bleeding(DUB)
in 33.9% , fibroid uterus in 24.6%, adenomyosis in 22.3%,
uterovaginal prolapse in 15.9%, post-menopausal bleeding in
2.8% and benign ovarian tumours in 0.5% of patients(Table
4).
Discussion
Various aetiologies have been proposed for the development
of adenomyosis, including genetic factors [6], increased intra-
uterine pressure as seen in the multipara, prior uterine surgery
[7,8], tamoxifen use [9] and hyperprolactinaemia. The true
prevalence of adenomyosis is still unknown. The prevalence
of adenomyosis in a study which was done by by Shaikh was
20.6 % [10] and it was 20.6% in a study which was done
by Ali [11]. Its incidence was shown to be 26 % in India by
Sharqill et al [12], 24.9% in Italy by Vercellin [13] and 6% in
West Indies by Raju et al [14]. In our study, the prevalence was
24.43%.
In a study by Anwar Ali, 73.7% of the patients were found
to be between 41-50 years of age,16.3% were between 31-
40 years of age, 1.6% were between 21-30 years of age and
8.1% were of >50 yrs of age [11]. In Swan’s study, the mean
age of the patients was 49.5± 3.4 [15]. In a study which was
done by Sabin, the percentage of the patients in the age
group of 41-50 years was found to be 70% and those in the
age group of 31-40 years was found to be 25.5%. Only 2%
of the patients were diagnosed with adenomyosis between
the ages of 21-30 years and 51-60 years [16]. In a study
which was done by Khresiat et al, 94% of the patients were
found to be more than 40 years of age [17]. These studies
were found to vary from our study in that almost equal num-
Volume : 4 | Issue : 3 | Mar 2015 ISSN - 2250-1991
7 | PARIPEX - INDIAN JOURNAL OF RESEARCH
bers of patients were diagnosed with adenomyosis in the age
group of 31-40 years and 41-50 years.
In a study by Weiss G et al, 58% of the patients were found
to have complaints of abnormal vaginal bleeding and 10%
had prolapse [15]. In Khreisat’s study, 64.71% of the pa-
tients had dysmenorrhoea, 70.5% had menorrhagia, 3.92%
had post-menopausal bleeding, 74.5% had dyspareunia, and
62.75% had chronic pelvic pain [17]. But in our study, men-
orrhagia was the predominant symptom in 75.6% of the pa-
tients and it was dysmenorrhoea in 33.3% of the patients.
In our study, adenomyosis was seen in 18.2% of patients
with prolapse and in 3.1% of patients with post-menopausal
bleeding. The menorrhagia may have been due to the dys-
functional contractility of the myometrium in patients with ad-
enomyosis.
In a study which was done by Khreisat, 96% of the patients
with adenomyosis had a parity of more than 3 [17]. The max-
imum occurrence was seen in patients with a mean parity of
3.8±2.3SD in a study [7] and it was 2.7 ±1.6 in another study
[8]. In our study, a majority of the patients were of parity 2
or 3. This correlated with the hypothesis that pregnancy may
facilitate the formation of adenomyosis by allowing the ade-
nomyotic foci to be included in the myometrium due to the
invasive nature of the trophoblasts on the extension of the
myometrial fibers. According to Reinhold, the specificity of the
preoperative diagnosis based on the clinical picture was poor,
ranging from 2.6–26% [2]. In our study, the clinical diagnosis
was DUB in 33.9%, fibroid in 24.6% and adenomyosis was
suspected in 22.3% of the patients.
Conclusion
The prevalence of adenomyosis is found to be 24.43% in
this study. Adenomyosis was diagnosed frequently in the age
group of 40-50 years in other studies while in our study wom-
en in the age group of 31-40 years and 41-50 years were
equally affected. The data which was obtained from interna-
tional studies were in consistence with those of our study re-
garding the parity and the symptoms of adenomyosis.
Adenomyosis is not a rare histopathological finding. Due to di-
agnostic and therapeutic methods which are being developed
as an alternative to hysterectomy, the clinical effects of ade-
nomyosis and its association with other gynaecological con-
ditions, adenomyosis appears to be an issue which should be
more intensively investigated in the future.
TABLES
TABLE1
AGE DISTRIBUTION OF ADENOMYOSIS UTERI
AGE NUMBER %AGE
21-30 8 2.1
31-40 153 39.2
41-50 183 46.9
51-60 42 10.8
>60 4 1.0
TOTAL 390 100
TABLE 2
PARITY DISTRIBUTION OF ADENOMYOSIS UTERI
PARITY NUMBER %AGE
0 10 2.6
1 12 3.1
2 145 37.2
3 160 41.0
4 46 11.8
5 17 4.3
TOTAL 390 100
TABLE 3
SYMPTOMS IN PATIENTS WITH ADENOMYOSIS UTERI
(There is overlap of symptoms)
SYMPTOMS NUMBER %AGE
Menorrhagia 295 75.6
Dysmenorrhoea 130 33.3
Pain Lower
Abdomen 35 8.9
Mass Descending
PV 71 18.2
Postmenopausal
Bleeding 12 3.1
Mass Abdomen 3 0.8
TABLE 4
CLINICAL DIAGNOSIS
DIAGNOSIS NUMBER %AGE
Fibroid 96 24.6
DUB 132 33.9
Adenomyosis 87 22.3
Postmenopausal
Bleeding 11 2.8
Uterovaginal
Prolapse 62 15.9
Ovarian Cyst 2 0.5
Total 390 100
(Fig. 1) Ectopic endometrial glands and stroma lying with-
in myometrium. H&E(40x10)
References
1. Azziz R. Adenomyosis: the current perspectives. Obstet Gynaecol Clin North Am | 1989;16: 221–35. | 2. Reinhold C, Tafazoli F, Wang L. The imaging features of adeno-
myosis. Hum Reprod Update 1998;4: 37–49. | 3. Parazzini F, Vercellini P , Panazza S, Chatenoud L, Oldani S, Crosignani PG. The risk factors for adenomyosis. Hum Reprod
1997; 12: 1275–9. | 4. Vavilis D, Agorastos T, Tzafetas J, Loufopoulos A, Vakiani M, Constantinidis T. Adenomyosis at hysterectomy: its prevalence and its relationship to
the operative findings and the reproductive and the menstrual factors. Clin Exp Obstet Gynaecol 1997; 24: 36–8. | 5. Cirpan T, Yeniel O, Ulukus M, Ozbal A, Gundem G,
Ozsener S, Mete Itil I, Zekioglu O. Clinical symptoms and histopathological findings in subjects with adenomyosis uteri. Clin Exp Obstet Gynecol. 2008;35(1): 48-53. | 6. Emge
LA. Elusive adenomyosis of the uterus. Its historical past and its present state of recognition. Am J Obstet Gynaecol 1962;83: 1541–63. | 7. Levgur M, Abadi MA, Tucker A.
Adenomyosis: symptoms, histology, and pregnancy terminations. Obstet Gynaecol 2000;95: 688–91. | 8. Panganamamula UR, Harmanli OH, Isik-Akbay EF, Grotegut CA,
Dandolu V, Gaughan JP . Is prior uterine surgery a risk factor for adenomyosis? Obstet Gynaecol 2004;104: 1034–38. | 9. Cohen I. A high frequency of adenomyosis in post
menopausal breast cancer patients who were treated with tamoxifen. Gynaecol Obstet Invest.1997; 44 (3): 200-5. | 10. Shaikh H, Khan KS. Adenomyosis in Pakistani wom-
en. Four years of experience at the Aga Khan University Medical Centre, Karachi. J Clin Pathol 1990; 43: 817-9. | 11. Ali A. The incidence of adenomyosis in hysterectomies.
Pak J Med Res 2005;44: 38-40. | 12. Sharqill SK, Sharqill HK, Gupta M, Kaur S. A clinicopathological study of hysterectomy. J Indian Med Assoc 2002; 100: 238- 9. | 13.
Vercellin P . Adenomyosis in hysterectomies: A study on the frequency distribution and the patient characteristics. Hum Reprod 1995;10: 1160-2. | 14. Raju GC, Narayn Singh
V, Jankey N. Adenomyosis uteri: A study of 416 cases. Aust NZ J Obstet Gynaecol 1988;28: 72-3. | 15. Weiss G, Maseelall P , Schott LL, Brockwell SE, Schocken M, Johnston
JM. Adenomyos is a variant, not a disease. Evidence from hysterectomized menopausal women in the Study of Women’s Health Across the Nation (SWAN). Fertil Steril. 2009
;91(1): 201-6. | 16. Ranabhat SK , Shrestha R , Tiwari M , Sinha DP , Subedee LR. A retrospective histopathological study of hysterectomy with or without salpingoophorec-
tomy specimens. JCMC 2010;1(1): 26-29. | 17. Khreisat B, Al-Rawabdeh S, Duqoum W. Adenomyosis: the frequency of hysterectomy in the histopathological specimens at
two Jordanian military hospitals JRMS 2011; 18(2): 76-79 . J Clin Pathol 1985; 38: 694-700. |
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