Cesarian scar endometriosis

Changed by Nikolaos-Achilleas Arkoudis, 5 Jan 2024
Disclosures - updated 5 Jan 2024: Nothing to disclose

Updates to Article Attributes

Body was changed:

Caesarian scar endometriosis is a term given to endometriosis occurring in a caesarian section scar. It can be located in the skin, subcutaneous tissue, rectus muscle/sheath, intraperitoneally, or in the uterine myometrium (within uterine scar).

Epidemiology

The reported incidence of abdominal scar endometriosis following caesarean section is 0.03-0.6% 6.

Clinical presentation

Patients may complain of tenderness to palpation and a raised, unsightly hypertrophic scar. Most patients have cyclical pain (up to 70%) 5. The pain is usually intermittent and associated with the patient's menstrual cycle but it may be constant in nature. Some reports state that only as low as 20% of the patients exhibited cyclical symptoms. The overlying skin may be hyperpigmented due to the deposition of haemosiderin. Some patients may be asymptomatic 4.

However, CT has limited use in the diagnosis of scar endometriosis given its limited contrast resolution and unnecessary radiation exposure 9. Therefore, in combination with the non-specific imaging manifestations it displays, it is not an imaging technique advised to be performed upon suspicion of this condition 13. Nevertheless, caesarian-section scar endometriosis may often clinically manifest as another disease (i.e., abdominal wall hernia, appendicitis, etc.) and thus be discovered incidentally with CT performed to exclude other diagnosis 9.

Pathology

It is thought to be caused by the implantation of endometrial stem cells at the surgical site at the time of uterine surgery.

To achieve a definitive diagnosis, histopathology is mandatory. It may detect endometrial-type glands, endometrial-type stroma, and/or haemosiderin-laden macrophages and must display two of the aforementioned three components 11.

Radiographic features

For general imaging features of endometriosis: refer to the parent article.

Imaging studies should ideally be carried out during the menstrual cycle 10.

In general, lesions found along the visible abdominal wall scar and along the predicted path of a previous caesarian section scar should initially raise concern for this diagnosis in imaging studies 9.

Ultrasound

Ultrasound may be of limited value if lesions have developed deeply within the abdominal cavity and are not superficially situated within the abdominal wall 8. Additionally, sonographic features are not specific. A subcutaneous nodule having relatively irregular borders, a heterogeneous, but predominantly hypoechoic echotexture with internal scattered hyperechoic echoes surrounded by a hyperechoic ring of variable width, and vascularity may be present. Occasionally cystic changes may be present 6.

Due to the nonspecific and frequently inconclusive sonography findings, ultrasound is primarily useful for image-guided tissue biopsy of suspected lesions and for confirming or ruling out other conditions included in the differential diagnosis 9. Those may include lipomas, suture granulomas, incisional or other types of abdominal wall hernias, etc 4. In most other situations, further imaging will be necessary.

CT

On CT imaging, they may appear as a solid soft-tissue mass with spiculated margins and mild/moderate enhancement after IV contrast material injection 9, 12. The lesions will usually be found close to and/or along the path of the previous caesarian scar.

However, CT has limited use in the diagnosis of scar endometriosis given its limited contrast resolution and unnecessary radiation exposure 9. Therefore, in combination with the non-specific imaging manifestations it displays, it is not an imaging technique advised to be performed upon suspicion of this condition 13. Nevertheless, caesarian-section scar endometriosis may often clinically manifest as another disease (i.e., abdominal wall hernia, appendicitis, etc.) and thus be discovered incidentally with CT performed to exclude other diagnosis 9

MRI

The most sensitive imaging modality. Often accurately locates the lesion in relation to a previous C-section scar, with signal characteristics similar to that of background endometriosis.

Typical MRI imaging features 9:

T2-weighted imaging

Mostly hypointense lesions that may display small hyperintense foci, a low signal rim (due to haemosiderin), and poorly defined infiltrative margins.

T1-weighted imaging

Intermediate or mildly hyperintense lesion with hyperintense-haemorrhagic foci both on non-fat-saturated and fat-saturated images and a low signal rim (due to haemosiderin). 

C+

Usually demonstrates contrast enhancement. Contrast-enhanced dynamic MRI may also be of assistance 16

DWI

Lesions may demonstrate restricted diffusion 10.

T2∗-weighted imaging

May further enhance the detection of haemosiderin given the increased sensitivity of this sequence to susceptibility artifacts 15.

Because of its larger field of view and reproducibility, MRI is better than ultrasound and can help identify more areas of endometriosis development 14. Furthermore, because of its greater tissue property characterisation and lack of ionising radiation, it is advantageous to CT 4.

Treatment and prognosis

Surgical excision with clear resection margins is the favoured treatment in symptomatic patients. Nevertheless, over the past few years, interventional radiology procedures using minimally invasive, percutaneous techniques (such as radiofrequency ablation, cryoablation, sclerotherapy, and high-intensity focused ultrasound) have also started to be implemented successfully, thus adding to the available treatment options 9.

Medical treatment with hormonal suppression (GnRH analogues) can offer temporary improvement in symptoms, with a low success rate 4

  • -<p><strong>Caesarian scar endometriosis</strong> is a term given to <a href="/articles/endometriosis">endometriosis</a> occurring in a caesarian section scar. It can be located in the skin, subcutaneous tissue, rectus muscle/sheath, intraperitoneally, or in the uterine myometrium (within uterine scar).</p><h4>Epidemiology</h4><p>The reported incidence of abdominal scar endometriosis following caesarean section is 0.03-0.6% <sup>6</sup>.</p><h4>Clinical presentation</h4><p>Patients may complain of tenderness to palpation and a raised, unsightly hypertrophic scar.&nbsp;Most patients have cyclical pain (up to 70%)&nbsp;<sup>5</sup>. The pain is usually intermittent and associated with the patient's menstrual cycle but it may be constant in nature. Some reports state that only as low as 20% of the patients exhibited cyclical symptoms.&nbsp;The overlying skin may be hyperpigmented due to the deposition of haemosiderin. Some patients may be asymptomatic <sup>4</sup>.</p><p>However, CT has limited use in the diagnosis of scar endometriosis given its limited contrast resolution and unnecessary radiation exposure <sup>9</sup>. Therefore, in combination with the non-specific imaging manifestations it displays, it is not an imaging technique advised to be performed upon suspicion of this condition <sup>13</sup>. Nevertheless, caesarian-section scar endometriosis may often clinically manifest as another disease (i.e., abdominal wall hernia, appendicitis, etc.) and thus be discovered incidentally with CT performed to exclude other diagnosis <sup>9</sup>.</p><h4>Pathology</h4><p>It is thought to be caused by the implantation of endometrial stem cells at the surgical site at the time of uterine surgery.</p><p>To achieve a definitive diagnosis, <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/histopathology" title="Learn more about histopathology from ScienceDirect's AI-generated Topic Pages">histopathology</a> is mandatory. It may detect endometrial-type glands, endometrial-type stroma, and/or haemosiderin-laden macrophages and must display two of the aforementioned three components <sup>11</sup>.</p><h4>Radiographic features</h4><p>For general imaging features of <a href="/articles/endometriosis">endometriosis</a>: refer to the parent article.</p><p>Imaging studies should ideally be carried out during the menstrual cycle <sup>10</sup>.</p><p>In general, lesions found along the visible abdominal wall scar and along the predicted path of a previous caesarian section scar should initially raise concern for this diagnosis in imaging studies <sup>9</sup>.</p><h5>Ultrasound</h5><p>Ultrasound may be of limited value if lesions have developed deeply within the abdominal cavity and are not superficially situated within the abdominal wall <sup>8</sup>. Additionally, sonographic features are not specific.&nbsp;A subcutaneous nodule having relatively irregular borders, a heterogeneous, but predominantly hypoechoic echotexture with internal scattered hyperechoic echoes surrounded by a hyperechoic ring of variable width, and vascularity may be present. Occasionally cystic changes may be present <sup>6</sup>.</p><p>Due to the nonspecific and frequently inconclusive sonography findings, ultrasound is primarily useful for image-guided tissue biopsy of suspected lesions and for confirming or ruling out other conditions included in the differential diagnosis <sup>9</sup>. Those may include lipomas, suture granulomas, incisional or other types of abdominal wall hernias, etc <sup>4</sup>. In most other situations, further imaging will be necessary.</p><h5>CT</h5><p>On&nbsp;CT imaging, they&nbsp;may&nbsp;appear&nbsp;as&nbsp;a&nbsp;solid&nbsp;soft-tissue mass&nbsp;with&nbsp;spiculated&nbsp;margins&nbsp;and&nbsp;mild/moderate&nbsp;enhancement&nbsp;after&nbsp;IV&nbsp;contrast&nbsp;material&nbsp;injection <sup>9, 12</sup>.&nbsp;The lesions will usually be found close to and/or along the path of the previous caesarian scar.</p><p>However, CT has limited use in the diagnosis of scar endometriosis given its limited contrast resolution and unnecessary radiation exposure <sup>9</sup>. Therefore, in combination with the non-specific imaging manifestations it displays, it is not an imaging technique advised to be performed upon suspicion of this condition <sup>13</sup>. Nevertheless, caesarian-section scar endometriosis may often clinically manifest as another disease (i.e., abdominal wall hernia, appendicitis, etc.) and thus be discovered incidentally with CT performed to exclude other diagnosis <sup>9</sup>.&nbsp;</p><h5>MRI</h5><p>The most sensitive imaging modality. Often accurately locates the lesion in relation to a previous C-section scar, with signal characteristics similar to that of background endometriosis.</p><h4>Treatment and prognosis</h4><p>Surgical excision with clear resection margins is the favoured treatment in symptomatic patients. Medical treatment with hormonal suppression (GnRH analogues) can offer temporary improvement in symptoms, with a low success rate <sup>4</sup>.&nbsp;</p>
  • +<p><strong>Caesarian scar endometriosis</strong> is a term given to <a href="/articles/endometriosis">endometriosis</a> occurring in a caesarian section scar. It can be located in the skin, subcutaneous tissue, rectus muscle/sheath, intraperitoneally, or in the uterine myometrium (within uterine scar).</p><h4>Epidemiology</h4><p>The reported incidence of abdominal scar endometriosis following caesarean section is 0.03-0.6% <sup>6</sup>.</p><h4>Clinical presentation</h4><p>Patients may complain of tenderness to palpation and a raised, unsightly hypertrophic scar.&nbsp;Most patients have cyclical pain (up to 70%)&nbsp;<sup>5</sup>. The pain is usually intermittent and associated with the patient's menstrual cycle but it may be constant in nature. Some reports state that only as low as 20% of the patients exhibited cyclical symptoms.&nbsp;The overlying skin may be hyperpigmented due to the deposition of haemosiderin. Some patients may be asymptomatic <sup>4</sup>.</p><p>However, CT has limited use in the diagnosis of scar endometriosis given its limited contrast resolution and unnecessary radiation exposure <sup>9</sup>. Therefore, in combination with the non-specific imaging manifestations it displays, it is not an imaging technique advised to be performed upon suspicion of this condition <sup>13</sup>. Nevertheless, caesarian-section scar endometriosis may often clinically manifest as another disease (i.e., abdominal wall hernia, appendicitis, etc.) and thus be discovered incidentally with CT performed to exclude other diagnosis <sup>9</sup>.</p><h4>Pathology</h4><p>It is thought to be caused by the implantation of endometrial stem cells at the surgical site at the time of uterine surgery.</p><p>To achieve a definitive diagnosis, <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/histopathology" title="Learn more about histopathology from ScienceDirect's AI-generated Topic Pages">histopathology</a> is mandatory. It may detect endometrial-type glands, endometrial-type stroma, and/or haemosiderin-laden macrophages and must display two of the aforementioned three components <sup>11</sup>.</p><h4>Radiographic features</h4><p>For general imaging features of <a href="/articles/endometriosis">endometriosis</a>: refer to the parent article.</p><p>Imaging studies should ideally be carried out during the menstrual cycle <sup>10</sup>.</p><p>In general, lesions found along the visible abdominal wall scar and along the predicted path of a previous caesarian section scar should initially raise concern for this diagnosis in imaging studies <sup>9</sup>.</p><h5>Ultrasound</h5><p>Ultrasound may be of limited value if lesions have developed deeply within the abdominal cavity and are not superficially situated within the abdominal wall <sup>8</sup>. Additionally, sonographic features are not specific.&nbsp;A subcutaneous nodule having relatively irregular borders, a heterogeneous, but predominantly hypoechoic echotexture with internal scattered hyperechoic echoes surrounded by a hyperechoic ring of variable width, and vascularity may be present. Occasionally cystic changes may be present <sup>6</sup>.</p><p>Due to the nonspecific and frequently inconclusive sonography findings, ultrasound is primarily useful for image-guided tissue biopsy of suspected lesions and for confirming or ruling out other conditions included in the differential diagnosis <sup>9</sup>. Those may include lipomas, suture granulomas, incisional or other types of abdominal wall hernias, etc <sup>4</sup>. In most other situations, further imaging will be necessary.</p><h5>CT</h5><p>On&nbsp;CT imaging, they&nbsp;may&nbsp;appear&nbsp;as&nbsp;a&nbsp;solid&nbsp;soft-tissue mass&nbsp;with&nbsp;spiculated&nbsp;margins&nbsp;and&nbsp;mild/moderate&nbsp;enhancement&nbsp;after&nbsp;IV&nbsp;contrast&nbsp;material&nbsp;injection <sup>9, 12</sup>.&nbsp;The lesions will usually be found close to and/or along the path of the previous caesarian scar.</p><p>However, CT has limited use in the diagnosis of scar endometriosis given its limited contrast resolution and unnecessary radiation exposure <sup>9</sup>. Therefore, in combination with the non-specific imaging manifestations it displays, it is not an imaging technique advised to be performed upon suspicion of this condition <sup>13</sup>. Nevertheless, caesarian-section scar endometriosis may often clinically manifest as another disease (i.e., abdominal wall hernia, appendicitis, etc.) and thus be discovered incidentally with CT performed to exclude other diagnosis <sup>9</sup>.&nbsp;</p><h5>MRI</h5><p>The most sensitive imaging modality. Often accurately locates the lesion in relation to a previous C-section scar, with signal characteristics similar to that of background endometriosis. </p><p>Typical MRI imaging features <sup>9</sup>:</p><h6>T2-weighted imaging</h6><p>Mostly hypointense lesions that may display small hyperintense foci, a low signal rim (due to haemosiderin), and poorly defined infiltrative margins.</p><h6>T1-weighted imaging</h6><p>Intermediate or mildly hyperintense lesion with hyperintense-haemorrhagic foci both on non-fat-saturated and fat-saturated images and a low signal rim (due to haemosiderin).&nbsp;</p><h6>C+</h6><p>Usually demonstrates contrast enhancement. Contrast-enhanced dynamic MRI may also be of assistance <sup>16</sup>.&nbsp;</p><h6>DWI</h6><p>Lesions may demonstrate restricted diffusion <sup>10</sup>.</p><h6>T2∗-weighted imaging</h6><p>May further enhance the detection of haemosiderin given the increased sensitivity of this sequence to susceptibility artifacts <sup>15</sup>.</p><p>Because of its larger field of view and reproducibility, MRI is better than ultrasound and can help identify more areas of endometriosis development <sup>14</sup>. Furthermore, because of its greater tissue property characterisation and lack of ionising radiation, it is advantageous to CT <sup>4</sup>. </p><h4>Treatment and prognosis</h4><p>Surgical excision with clear resection margins is the favoured treatment in symptomatic patients. Nevertheless, over the past few years, interventional radiology procedures using minimally invasive, percutaneous techniques (such as radiofrequency ablation, cryoablation, sclerotherapy, and high-intensity focused ultrasound) have also started to be implemented successfully, thus adding to the available treatment options <sup>9</sup>.</p><p>Medical treatment with hormonal suppression (GnRH analogues) can offer temporary improvement in symptoms, with a low success rate <sup>4</sup>.&nbsp;</p>

References changed:

  • 14. Jha P, Sakala M, Chamie L et al. Endometriosis MRI Lexicon: Consensus Statement from the Society of Abdominal Radiology Endometriosis Disease-Focused Panel. Abdom Radiol. 2019;45(6):1552-68. <a href="https://doi.org/10.1007/s00261-019-02291-x">doi:10.1007/s00261-019-02291-x</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/31728612">Pubmed</a>
  • 15. Foti P, Farina R, Palmucci S et al. Endometriosis: Clinical Features, MR Imaging Findings and Pathologic Correlation. Insights Imaging. 2018;9(2):149-72. <a href="https://doi.org/10.1007/s13244-017-0591-0">doi:10.1007/s13244-017-0591-0</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/29450853">Pubmed</a>
  • 16. Onbas O, Kantarci M, Alper F et al. Nodular Endometriosis: Dynamic MR Imaging. Abdom Imaging. 2007;32(4):451-6. <a href="https://doi.org/10.1007/s00261-006-9038-7">doi:10.1007/s00261-006-9038-7</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/17420957">Pubmed</a>

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