Endometriosis, Cicatrix, Abdominal wall, Gynecologic surgical
procedures, Menstruation -associated disorders
Received: 2025/05/22
Accepted: 2025/06/26
Published Online: 05 Sep. 2025
Corresponding Information:
Karthiga Prabhu,
Department of Obstetrics and Gynecology,
SRM Medical College Hospital and Research
Center, Chengalpattu, India
Email:
[email protected]
Copyright © 2025, This is an original open -access article distributed under the terms of the Creative Commons Attribution-noncommercial
4.0 International License which permits copy and redistribution of the material just in noncommercial usages with proper citation .
1. Introduction
Endometriosis is characterized by the existence of
functional endometrial glands and stroma located
outside the uterine cavity, commonly presenting as
chronic pelvic pain or infertility in women of
childbearing age (1). While endometriosis primarily
affects pelvic organs (such as ovaries, peritoneum, and
uterosacral ligaments), ectopic endometrial tissue can
also develop in areas outside the pelvis, including the
abdominal wall, surgical scars, gastrointestinal tract, or
thoracic cavity (2). Scar endometrio sis refers to the
implantation of endometrial tissue in or near a surgical
scar, most frequently occurring after obstetric or
gynecologic procedures (1). This condition is quite
uncommon, as abdominal wall endometriomas make
up less than 1% of all endometriosis cases. The
occurrence of scar endometriosis after cesarean
delivery ranges from 0.03% to 0.8% in women
undergoing a previous Cesarean section (2).
The development of scar endometriosis is due to the
iatrogenic transplantation of endometrial cells during
surgical intervention. Viable endometrial cells from the
uterus might be introduced into the incision (for
instance, during uterine incision closure in a Cesarean
section or other uterine surgeries) where these cells
could implant and eventually grow under hormonal
influences (3). Over time, these implants can develop
their own blood supply and may experience cyclical
bleeding, resulting in the formati on of a localized
endometrioma within the scar tissue. The risk factors
include any surgical procedures that compromise the
uterine cavity or fallopian tubes while endometrial
tissue is present. Cesarean sections are the most
frequently seen precursor, although cases have b een
documented after procedures like hysterotomy for
termination, myomectomy, tubal ligation, and even
episiotomies (3,4). A delay of several years between
the initial surgery and the onset of symptoms is
common, with an average interval of around 3 to 5
years in various studies (1,4).
In clinical practice, scar endometriosis typically
manifests as a palpable subcutaneous nodule located at
or near a scar, often accompanied by localized pain that
worsens during menstruation (3). Patients may observe
a cyclical increase in size or tenderness of the mass at
regular intervals. In rare cases, when the endometriotic
tissue invades the dermis or epidermis, there can be
actual bleeding or menstrual -like discharge from the
scar, illustr ating the “menstruating scar” effect (5).
Since there are various symptoms, which can resemble
more common surgical conditions (such as incisional
hernias, stitch granulomas, abscesses, or tumors),
diagnosis frequently suffers delays or is overlooked
(5). Here, we report a case of scar endometriosis in a
young woman who had a tubal ligation scar and
experienced cyclical bleeding from the surface of the
scar.
Giddaluru Bhavya Muralikrishna, et al. 804
Volume 10, October 2025 Journal of Obstetrics, Gynecology and Cancer Research
2. Case Presentation
A 28-year-old female (gravida 3, para 2) visited the
gynecology clinic with a two -year history of recurring
pain and bleeding from lower abdominal scar during
menstrual cycles. She reported experiencing sharp pain
at surgical scar site for the first 2-3 days of each period,
along with spotting blood from the scar itself. The
menstrual cycles were regular (30 -35 days apart,
lasting 3 days) with a normal volume and minimal
dysmenorrhea apart from the localized pain at the scar.
She had two previous full -term normal vaginal births.
In 2018, the patient had a first -trimester surgical
evacuation due to missed miscarriage, combined with
a bilateral tubal ligation via a mini -laparotomy
approach. The scar from that surgery was
approximately a 5 cm Pfannenstiel -Kerr incision
located just above the pubic symphysis. The onset of
cyclic scar pain began roughly a year after that surgical
procedure and progressively intensified, while blood
staining at the scar synchronized with menstrual cycles
appeared around a year late r. She did not report any
other significant medical or surgical history.
Upon examination, the patient had stable vital signs.
Abdominal inspection showed a well-healed transverse
suprapubic scar. At the center of this scar was a nodular
swelling approximately 3×3 cm in size, with a slight
bluish-brown discoloration of the ove rlying skin. A
trace of blood was observed oozing from a pinpoint
area in the scar during the second day of her
menstruation ( Figure 1). Palpation revealed a firm,
tender nodule fixed to the abdominal wall at the scar
site; no herniation was present, and t he remaining
abdomen was soft and non -tender. The pelvic
examination was normal, showing a typical sized
anteverted uterus without any adnexal masses or
tenderness.
Ultrasonography of the abdominal wall revealed an
ill-defined, irregular heterogeneously hypoechoic
lesion about 3 cm in size located in the subcutaneous
tissue of the abdominal wall, adjacent to the rectus
muscle, with internal vascularity noted on Dopple r
imaging (indicative of an endometriotic implant)
(Figure 2). MRI of the abdomen and pelvis was
performed for improved anatomical visualization that
showed a well -defined solid mass measuring
4.4×3.5×2.7 cm in the subcutaneous area of the right
lower abdo minal wall (at the site of the tubectomy
scar). The lesion appeared isointense on T1 -weighted
images and hypointense on T2 -weighted images, with
no signs of deeper extension beyond the anterior rectus
sheath or into the peritoneal cavity ( Figure 3). These
imaging characteristics were compatible with a
subcutaneous endometriosis (endometrioma) localized
to the abdominal wall. The MRI findings, along with
the lesion’s location, strongly suggested scar
endometriosis.
Considering the patient's history and the clinical and
radiological results, scar endometriosis was diagnosed.
It was decided to proceed with surgical intervention.
The patient underwent wide local excision of the
abdominal wall endometriotic mass under re gional
anesthesia. A curved incision was made around the
existing scar, encompassing the entire palpable nodule
along with a margin of healthy tissue. During the
surgery, a 4×4 cm firm mass was dissected from the
surrounding subcutaneous tissues and excise d en bloc
down to the level of the rectus sheath. The lesion was
tightly adherent to the rectus fascia, necessitating the
removal of a portion of the sheath without
fragmentation to ensure clear margins. Following
excision, the cut surface of the mass show ed areas of
fibrosis containing “chocolate -colored” fluid and old
blood debris, including a few bluish punctate spots
within the tissue - a gross morphology consistent with
an endometriotic tumor (Figure 4). The abdominal wall
defect was repaired with interrupted 1-0 polypropylene
(Prolene) sutures to close the fascial layer, and the skin
was sutured with nylon. The postoperative course was
uneventful, and the patient made a good recovery.
Histopathological analysis of the excised tissue
confirmed the diagnosis. On gross examination, the
specimen was a fibro fatty nodule exhibiting cystic
degeneration filled with old blood. Microscopic
examination using hematoxylin and eosin staining
revealed endometrial glandular epithelium organizing
into glands and cystic structures, surrounded by
endometrial stromal cells embedded within fibro
collagenous scar tissue and adjacent muscle. Evidence
of hemorrhage and a sinus tract extending to the skin
surface, with surrounding granulation tissue, correlated
with the clinically observed bleeding sinus ( Figure 5).
These findings established the diagnosis of
endometriosis in the scar. The patient was discharged
on postoperative day 2 with stable vital signs and a
clean surgical wound. She received instructions for
routine postoperative care, including daily dressi ng
changes, suture inspection, and medications such as
oral analgesics and antibiotics (Amoxicillin-clavulanic
acid 625 mg twice daily for 5 days). Act ivity
restrictions included avoiding heavy lifting and
strenuous abdominal exercises for 4 -6 weeks, with
suture removal on day 7. A clinical review was
scheduled for 1 and 3 months postoperatively. Since
the lesion was entirely excised and the patient wanted
to preserve fertility, no hormonal therapy was started.
She was informed about signs of recurrence and
instructed to report any pain, swelling, or bleeding
from the scar.
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Volume 10, October 2025 Journal of Obstetrics, Gynecology and Cancer Research
Figure 1. Clinical image- Abdominal scar examination
Figure 2. Ultrasound image showing a heterogeneously hypoechoic, ill-defined lesion in the subcutaneous plane, with internal
vascularity (color Doppler). The lesion is located at the site of the surgical scar and abuts the rectus abdominis muscle
Figure 3. Pelvic MRI showing an anterior abdominal wall lesion (pink arrows) at the site of the prior Pfannenstiel incision.
On T1-Weighted (T1W) images (top left), the lesion appears isointense; On T2 -weighted (T2W) images (top right), the
lesion appears hypointense characteristic of endometriotic tissue with fibrotic and hemorrhagic components. No extension
into the peritoneal cavity or underlying muscle was noted.
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Volume 10, October 2025 Journal of Obstetrics, Gynecology and Cancer Research
Figure 4. Intraoperative Image- Excised Abdominal Wall Endometriotic Mass. The cut surface reveals fibrotic areas
interspersed with brownish, chocolate-colored hemorrhagic fluid and cystic spaces- characteristic of endometriotic tissue.
Figure 5. Histopathological examination of the excised scar nodule reveals endometrial glands (indicated by the arrow)
surrounded by endometrial stroma and a sinus tract along with granulation tissue development underneath.
3. Discussion
Scar endometriosis is a rare complication of obstetric
or gynecologic surgery, with the most frequently
affected area being Cesarean section scars (6). The
estimated incidence of endometriosis in a cesarean scar
range from 0.2% to 0.8%, although some extensive
reviews suggest a broader range of approximately
0.03% to 0.45% (1,6). This condition often remains
undiagnosed due to its infrequency and ability to
imitate other post-surgical lesions. In the present case,
the patient’s history of undergoing tubal ligation (mini
laparotomy) likely triggered the introduction of
endometrial tissue into the abdominal wall. Although
cesarean delivery is the typical r isk factor, there have
also been instances of scar endometriosis following
procedures like abdominal tubal sterilization,
hysterotomy for abortion, myomectomy, or even
laparoscopy, essentially any surgical procedure that
could implant endometrial cells int o a wound. Not
every surgical contamination results in endometriosis,
indicating that other factors (such as individual
susceptibility or immune and hormonal influences) are
involved in whether implanted cells will grow. Some
evidence suggests a genetic te ndency towards
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Volume 10, October 2025 Journal of Obstetrics, Gynecology and Cancer Research
developing endometriosis at ectopic sites, but the
prevailing theory for the pathogenesis of scar
endometriosis is direct implantation during surgery
combined with subsequent hormonal stimulation of the
implants (7,8). Classic theories pertaining to the
pathogenesis of pelvic endometriosis such as
Sampson’s retrograde menstruation and coelomic
metaplasia are less applicable to scar endometriosis,
except in cases where endometrial tissue may access a
scar through tubal reflux (as was previously
hypothesized regarding endometriosis following tubal
ligation). In our patient, it appears that endometrial
tissue from the uterine cavity or fallopian tubes was
unintentionally deposited into the abdominal wall
incision during the tubal ligation, remaining dormant
until factors such as estrogen -progesterone cycles
encouraged its growth.
Patients with scar endometriosis usually present with
a palpable mass at or close to the scar and pain often
corresponding with menstrual cycle. A review of 198
cases of cesarean scar endometriosis indicated that
approximately 87% of patients experienced c yclical
pain associated with menstruation, while a smaller
percentage reported continuous or non -cyclical pain
(5). The duration from the initial surgery to the onset
of symptoms can vary widely, averaging about 2 to 5
years (3). Interestingly, our patient experienced the
symptoms relatively sooner (within 1 to 2 years),
possibly due to the smaller incision and the closer
proximity of endometrial tissue to the skin surface in a
tubectomy scar. Visible bleeding from the scar, as
observed in our patient, is u ncommon but has been
documented when endometriotic lesions involve the
epidermis. This striking symptom can aid in the
diagnosis, as scar endometriosis is more frequently
mistaken with other conditions. The differential
diagnosis for an abdominal wall mass in a woman with
prior pelvic surgery includes incisional hernia, surgical
site hematoma or abscess, suture granuloma, desmoid
tumor, lipoma, or metastatic tumor implant (9).
Recognizing the cyclical nature of the symptoms is
crucial for differentiating scar endometriosis from
other conditions. In the present case, the occurrence of
menstrual bleeding from the scar was a clear indicator
suggesting endometriosis and helped pre vent
confusion in diagnosis.
The assessment of suspected scar endometriosis
requires an integration of patient history and
examination with imaging studies and tissue analysis.
Ultrasound serves as a valuable initial imaging
technique: a scar endometrioma usually presents as a
solid o r mixed solid -cystic mass that appears
hypoechoic compared to fat and may include internal
echogenic spots or fluid -filled areas resulting from
bleeding (10). Doppler ultrasound frequently reveals
internal blood flow. In our patient, a heterogeneous
vascular mass within the subcutaneous layer was
observed in the ultrasound, which, considering the
clinical context, was consistent with an endometriotic
lesion. MR I can be particularly advantageous for
detailing the extent of the lesion and any nearby
structure involvement. On MRI, lesions of scar
endometriosis typically exhibit signal patterns akin to
hemorrhagic tissue- they can be isointense or slightly
hyperintense on T1 -weighted images, with regions of
hyperintensity if there is acute bleeding present and are
generally hypointense on T2 -weighted images due to
dense fibrosis and hemosiderin accumulation (3). In
our patient, MRI confirmed that the endometriotic
mass was restricted to the abdominal wall and there
was no infiltration into the peritoneal cavity, which was
significant for surgical planning.
While imaging outcomes can strongly indicate the
diagnosis, histopathology provides ultimate
confirmation. A preoperative core needle biopsy or
Fine-Needle Aspiration Cytology (FNAC) can reveal
endometrial cells within the mass, though this is not
always requisite if the clinical picture is evident, and
some surgeons choose to avoid needle biopsy due to
worries about potential tissue seeding along the tract.
When conducted, FNAC has demonstrated high
sensitivity (close to 100% in certain studies) for
detecting scar endometriosis, showcasing clusters of
endometrial glandular cells, stromal cells, and
hemosiderin-loaded macrophages in cytological
preparations (11). In one investigation, all cases of scar
endometriosis undergoing FNAC were accurately
identified cytologically (12). In the current case, due to
the clear clinical cyclical bleeding and the correlation
with imaging, we advanced directly to excisional
surgery without FNAC. Definitive histological analysis
of the excised tissue showed the presence o f
endometrial glands and stroma, which is diagnostic for
endometriosis. Histology typically reveals surrounding
inflammation, fibrosis, and pigment -laden
macrophages resulting from recurrent bleeding (3). It
is crucial that both endometrial glands and stroma are
found in the sample to affirm the diagnosis; otherwise,
the findings could indicate other conditions (for
instance, isolated endosalpingiosis or a stromal
nodule).
Surgery is the main treatment for scar endometriosis.
The optimal approach is wide local excision of the
lesion with clear margins, which offers the best chance
of resolution. Medical treatment (like hormonal
suppression via oral contraceptives, progestins ,
danazol, or GnRH analogues) has limited effectiveness
in scar endometriosis - it may temporarily alleviate
symptoms but generally does not eliminate the lesion
(12). In our patient, surgical removal of the lesion was
successful, as documented cases. A mar gin of at least
1 cm of healthy tissue surrounding the lesion is often
advised to ensure complete excision. If the
endometrioma affects the fascia or muscles, those parts
should be surgically removed; large defects might
require mesh repair or tissue flap reconstruction in
certain scenarios. In this case, the mass was excised
completely along with part of the rectus sheath, and the
defect was small enough to be primarily closed. After
thorough excision, the recurrence of scar endometriosis
Giddaluru Bhavya Muralikrishna, et al. 808
Volume 10, October 2025 Journal of Obstetrics, Gynecology and Cancer Research
is extremely uncommon. Research has indicated a low
rate of recurrence when wide excision with clear
margins is accomplished (1). On the other hand,
incomplete resection or spillage of endometrial tissue
during the operation can cause either persistence or
recurrence of the disease. Postoperative adjunct
therapy is not typically necessary, but some healthcare
providers choose to initiate hormonal suppression (like
a course of GnRH agonists or ongoing oral
contraceptives) after surgery to reduce the risk of
microscopic foci returning, particularly if the resection
margins were narrow (12). In our patient, due to the
clear margins and her wish for future pregnancies, no
medical suppression was administered, and she
remained symptom -free. A developing non -surgical
approach for treating abdominal wall endometriosis in
specific cases is High-Intensity Focused Ultrasound
(HIFU) ablation, which can thermally eliminate the
ectopic tissue without causing an incision (9).
Nevertheless, surgical intervention remains the
definitive and most effective treatment for accessible
lesions.
4. Conclusion
This case report emphasizes that the combination of
cyclical pain, a nodular mass located in or near a scar,
and a correlation with menstrual cycles strongly
indicates scar endometriosis. An accurate diagnosis
requires a thorough medical history and physic al
examination, along with appropriate imaging and
confirmation through histopathology. The definitive
solution involves the surgical removal of the lesion
with clear margins, which not only relieves symptoms
but also prevents recurrence.
5. Declarations
Acknowledgments
The authors would like to thank the Department of
Obstetrics and Gynecology at SRM Medical College
Hospital and Research Centre for their support in
managing the patient and facilitating the preparation of
this manuscript. We also acknowledge the patient f or
providing informed consent and permitting the
publication of clinical details and images.
Ethical Considerations
Informed written consent was obtained from the
patient for the publication of this case report and any
accompanying images. Ethical approval was not
required for this single -patient case report as per
institutional guidelines, as no experimental
intervention was involved.
Authors' Contributions
Bhavya Giddaluru contributed to the
conceptualization, clinical management, manuscript
drafting, and image documentation. Karthiga Prabhu
performed clinical supervision, surgical intervention,
and manuscript revision.
Conflict of Interest
The authors declare no conflict of interest regarding
the publication of this case report.
Fund or Financial Support
This study received no external financial support.
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