| Literature DB >> 24089684 |
Márcia Mendonça Carneiro1, Ivone Dirk de Sousa Filogônio, Luciana Maria Pyramo Costa, Ivete de Ávila, Márcia Cristina França Ferreira.
Abstract
BACKGROUND: Endometriosis is a chronic benign gynecologic disease that can cause pelvic pain and infertility affecting almost 10% of reproductive-age women. Deeply infiltrating endometriosis (DIE) is a specific entity responsible for painful symptoms which are related to the anatomic location of the lesions. Definitive diagnosis requires surgery, and histological confirmation is advisable. The aim of this paper is to review the current literature regarding the possibility of diagnosing DIE accurately before surgery. Despite its low sensitivity and specificity, vaginal examination and evaluation of specific symptoms should not be completely omitted as a basic diagnostic tool in detecting endometriosis and planning further therapeutic interventions. Recently, transvaginal ultrasound (TVUS) has been reported as an excellent tool to diagnose DIE lesions in different locations (rectovaginal septum, retrocervical and paracervical areas, rectum and sigmoid, and vesical wall) with good accuracy.Entities:
Mesh:
Year: 2013 PMID: 24089684 PMCID: PMC3780473 DOI: 10.1155/2013/564153
Source DB: PubMed Journal: Biomed Res Int Impact factor: 3.411
Relationship between type of chronic pelvic pain (CPP) and deeply infiltrating endometriosis (DIE) lanatomic location.
| Author | Type of study ( | Relationship between pain and DIE |
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| Cornillie et al. (1990) [ | Observational, prospective ( | Pelvic pain was strongly associated with deep lesions (>10 mm). |
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Koninckx et al. (1991) [ | Observational, prospective ( | DIE was strongly associated with pelvic pain, and depth of the lesion was the main factor associated with pain. |
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Perper et al. (1995) [ | Double blind observational, prospective ( | The intensity of menstrual pain is related to the number of endometrial implants in patients with endometriosis with either pelvic pain or infertility. No diagnosis of DIE. |
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Vercellini et al. (1996) [ | Observational, prospective ( | Presence of vaginal lesions was associated frequently with severe deep dyspareunia. Stage was not related to pain symptoms. |
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| Porpora et al. (1999) [ | Observational, prospective ( | Deep endometriosis, pelvic adhesions, and ovarian cystic endometriosis were independent predictors of pelvic pain. |
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Fauconnier et al. (2002) [ | Obsevational, retrospective ( | The frequency of dyspareunia increased with a uterosacral ligament DIE location. |
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| Chapron et al. (2003) [ | Observational, prospective/retrospective ( | The presence of a rectal or vaginal infiltration by the posterior DIE and extensiveness of adnexal adhesion were related to dysmenorrhea severity. |
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| Chapron et al. (2005) [ | Observational, prospective ( | The presence of a rectal or vaginal infiltration by the posterior DIE and extensiveness of adnexal adhesion were related to dysmenorrhea severity. |
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| Vercellini et al. (2007) [ | Observational, prospective ( | A strong association was found between posterior cul-de-sac lesions and dyspareunia. The association between endometriosis stage and severity of pelvic symptoms was marginal and inconsistent and could be demonstrated only with a major increase in study power. |
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| Seracchioli et al. (2008) [ | Retrospective ( | Severity of dyschezia was significantly correlated with posterior DIE. A positive correlation occurred between severity of dyschezia and lesion diameter with rectovaginal endometriosis but not with anterior rectal wall involvement. |
Figure 1Deeply infiltrative endometriosis lesion of the bowel on ultrasound.
Figure 2Deeply infiltrating endometriotic lesion of the right uterosacral ligament (arrow) at TVUS. Transversal view of the uterus, at the level of the upper third of the cervix.
Studies evaluating the accuracy of TVUS for the diagnosis of deeply infiltrating endometriosis in different locations.
| Locations studies | Rectovaginal septum | Bowel | Pouch of douglas | Retrocervical area | Uterosacral ligaments | Vagina | Bladder | ||||||||||||||
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| sp |
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Bazot et al., 2003 [ | 95 | 100 | 97 | 82 | 100 | 87 | 75 | 83 | 77 | 25 | 100 | 90 | |||||||||
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Abrao et al., 2007 [ | 98 | 100 | 99 | 95 | 98 | 97 | |||||||||||||||
| Menada et al., 2008 [ | 93 | 90 | 92 | 56 | 92 | 83 | |||||||||||||||
| *RWC | 97 | 100 | 98 | 96 | 100 | 99 | |||||||||||||||
| Piketty et al., 2008 [ | 91 | 96 | NR | ||||||||||||||||||
| Guerriero et al., 2008 [ | 74 | 88 | NR | 67 | 92 | NR | 50 | 94 | NR | 91 | 89 | NR | 100 | 100 | NR | ||||||
| Bazot et al., 2009 [ | 9 | 99 | 88 | 94 | 100 | 96 | 78 | 67 | 77 | 47 | 95 | 79 | |||||||||
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Goncalves et al., 2010 [ | 97 | 100 | 99 | ||||||||||||||||||
s: sensitivity (%); sp: specificity (%); a: accuracy (%); NR: not reported.
*RWC: after instillation of rectal water contrast.