Indian Journal of Pathology and Oncology 2021;8(4):522–525
Content available at: https://www.ipinnovative.com/open-access-journals
Indian Journal of Pathology and Oncology
Journal homepage: www.ijpo.co.in
Case Report
Serous borderline tumour of the peritoneum- A rare entity
Sandhyarani Mahadev Kanna
1,
*, Nidha Gaffoor
1
, Himasree E
1
, Nikhil P V
1
,
Archana Shetty
1
, Supriya Sandeepa
1
, Bhargavi K N
1
1
Dept. of Pathology, Dr Chandramma Dayanand Sagar Institute of Medical Sciences & Research, Ramnagara, Karnataka, India
ARTICLE INFO
Article history:
Received 11-08-2021
Accepted 18-09-2021
Available online 23-11-2021
Keywords:
Mesothelial hyperplasia
Primary peritoneal carcinoma
Serous borderline tumor
ABSTRACT
Serous borderline tumor is a rare entity of peritoneum which can lead to diagnostic dilemma due to
its resemblance with reactive lesions of peritoneum and ovarian borderline and malignant neoplasms.
Complete clinical details, histopathological evaluation and immunohistochemistry aid in arriving at correct
diagnosis. Recognizing this entity is important as it carries good prognosis.
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1. Introduction
Serous borderline tumor (SBT) of the peritoneum is
a rare low grade proliferative serous epithelial tumor,
fundamentally arising in the peritoneum,
1
without
underlying tissue invasion.
2
In SBT of the peritoneum,
bilateral ovaries and fallopian tubes are macroscopically
and microscopically normal. Ovary may show minimal
ovarian cortical involvement less than 5 × 5 mm
2
.
2
Prior to
the establishment of the term “SBT peritoneum”, various
other nomenclatures were utilized to describe this entity,
such as primary papillary peritoneal neoplasia, atypical
endosalpingiosis and peritoneal serous micropapillomatosis
of low malignant potential.
3
Serous borderline tumor is
an incidental finding most of the time during laparoscopic
procedures done for other clinical indications.
2. Case Report
A 20-year old unmarried female patient presented to
the Obstetric and Gynaecology department with irregular
menstrual cycles since 1 year. She had no history of
pain abdomen, dysmenorrhea, urinary or bowel symptoms.
* Corresponding author.
E-mail address: doc.sandhyamadhu@gmail.com (S. M. Kanna).
There was no history of loss of weight or loss of
appetite and no previous history of tuberculosis. Past
history revealed inguinal hernioplasty at 9 years of age.
There was no history of any malignancy in the family
members. Ultrasonography abdomen and pelvis showed
normal sized uterus, retroverted, endometrial thickness
of 5.8mm. Multiple intercommunicating oblong cystic
lesions with internal septations were separately seen from
right ovary collectively measuring 5.2 x 4.2cm with a
possibility of paraovarian cyst. No free fluid or lymph node
enlargement was noted. Bilateral adnexae were normal.
CA 125 was within normal limits. After pre-anesthesia
checkup, covid testing and informed written consent, patient
was taken up for surgery under general anesthesia for
diagnostic and therapeutic cystectomy. A retroperitoneal
multiloculated cyst (7x6 cms) was noted. Laparoscopic
cystectomy and marsupialization of the cyst was performed.
Clear serous fluid was drained. Inner surface of cyst was
smooth with no papillary excrescences. Separate small
papillary excrescences with calcific material approximately
5mm across were seen throughout the pelvis especially
on the right ovary, pouch of Douglas, and uterosacral
ligaments. Left ovary was unremarkable. There were no
adhesions in pelvis. A differential diagnosis of miliary
https://doi.org/10.18231/j.ijpo.2021.109
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