Introduction
Endometriosis is defined as the presence of endometrial glands and
stroma outside the uterine cavity1,2 and is thought to affect up to 10%
of women.3 Endometriotic lesions can be found anywhere in the body,
common sites are the ovaries, pelvic peritoneum and fallopian tubes.
It is less commonly found at the cervix, bladder, lungs and bowel.4
An association between endometriosis and malignancy has been
well documented in literature despite reported controversy of the
relationship.5,6 Brinton et al. 7 evaluated a large cohort of Swedish
women (20,868) with a diagnosis of endometriosis, were an
increased risk of cancer was found; in particular ovarian, breast and
haematopoietic malignancies. Reports of endometriosis associated
with cancers of the bowel are rare.
Appendicular tumours are rare and account for only 0.4% of all
gastrointestinal tumours. 8 They are usually found incidentally or
during investigations for other disease processes (as in our case),
accounting for 1% of appendectomies.9
Reports of endometriosis associated with bowel cancer are rare.
One similar case has been reported by Azordgean et al., 10 which
documented the coexistence of a carcinoid tumour of the appendix
and ileal endometriosis, each found at separate locations. 10 This
case presented with right lower abdominal pain mimicking acute
appendicitis and was treated surgically with excision of the ileum and
appendix. We describe the unique, not yet reported case of a 36 year
old woman presenting with primary infertility, who was found to have
a mucinous cyst-adenoma and carcinoid tumour of the appendix with
co-existent endometriosis.
Case presentation
A 36 year old asymptomatic woman was referred with a 3 year
history of primary infertility. Her periods occurred every 35-38 days
with an average bleed and she engaged in regular unprotected coitus.
No other personal or family medical history was noted and she led a
healthy lifestyle as a non-smoker with minimal alcohol intake.
Routine infertility tests for herself and her partner were mostly
normal. Except her ultrasound scan revealed 3-4 endometriotic
cysts in the right ovary, the largest being 3.5cm in diameter with a
small cyst also found in the left ovary. Endocervical swabs revealed
Chlamydia which was promptly treated. It was decided to proceed
with a diagnostic laparoscopy with tubal patency dye test and excision
of endometriosis if appropriate.
Obstet Gynecol Int J. 2014;1(1):5‒7. 5
©2014 Dunkerton. This is an open access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and build upon your work non-commercially.
Combined mucinous cystadenoma and carcinoid
tumour of the appendix with coexistent features of
an endometrioma: a case report
Volume 1 Issue 1 - 2014
Suzanna Dunkerton,1 Neena K Pankhania,1
Chris Johnson,2 T erek Gelbaya1
1Gynaecology, Leicester Royal Infirmary, UK
2Pathology, Leicester Royal Infirmary, UK
Correspondence: Suzanna Dunkerton, Leicester General
Hospital, Leicester, Leics, UK, T el 07979591333,
Email
Received: August 15, 2014 | Published: August 20, 2014
Abstract
Introduction: Endometriosis is defined as ‘the presence of endometrial glands and
stroma outside the uterine cavity’. Appendiceal cancers are rare tumours of the
gastrointestinal tract. There are some reported cases of these two disease processes
occurring simultaneously within separate lesions. However, there are no reported
cases of the two diseases occurring within the same entity. We report the unique case
of an appendiceal cancer (combined mucinous cyst adenoma and carcinoid tumour)
with coexistant histological features of an endometrioma.
Case report: A 36 year old nulliparous woman was referred to clinic with primary
infertility, with an unremarkable past medical history. After routine infertility
investigations, diagnostic laparoscopy was carried out and endometriosis was
diagnosed. A suspicious lesion was also seen on the appendix. A right hemicolectomy
and appendectomy was performed. Histological results showed mucinous cystadenoma
with well differentiated carcinoid tumour and coexistent features of an endometrioma.
Discussion
An association between endometriosis and cancer has been well
documented in literature. Existence with appendiceal cancers is rare. Carcinoids and
cyst adenomas are both common types of appendiceal cancers, found incidentally or
mimicking acute appendicitis. Occurrence in the same lesion is rare and unique to be
found with features of an endometrioma.
Conclusion
This case illustrates the broad spectrum of appendiceal and endometrial
disease. We hope to highlight the interesting asymptomatic presentation of this patient
and therefore the importance of requesting routine histopathological analysis after
appendicectomy.
Keywords
endometrioma, appendix, mucinouscystadenoma
Obstetrics & Gynecology International Journal
Case Report
Open Access
Combined mucinous cystadenoma and carcinoid tumour of the appendix with coexistent features of an
endometrioma: a case report
6
Copyright:
©2014 Dunkerton et al.
Citation: Dunkerton S, Pankhania NK, Johnson C, et al. Combined mucinous cystadenoma and carcinoid tumour of the appendix with coexistent features of
an endometrioma: a case report. Obstet Gynecol Int J . 2014;1(1):5‒7. DOI: 10.15406/ogij.2014.01.00001
Diagnostic laparoscopy found extensive uterovesical, peritoneal
and ovarian endometriosis.
Figure 1: Right lateral bowel adhesions were dissected and
endometriomas were excised from both ovaries and were mobilised as
per RCOG guidelines.2 The dye test revealed the left tube was patent
and the right blocked. Overall, grade 4 endometriosis was noted. On
further visualisation of the abdomen, a suspicious looking mucoid
lesion on the tip of the appendix was seen and biopsied.
Figure 1 Endometriosis seen at initial laparoscopy.
Figure 2: Histology of the appendix tip showed mucinous
Material
within the bowel wall and stroma suggesting a mucocele or
mucinous tumour of the appendix. The patient was referred to lower
gastrointestinal surgeons. A CT scan found it difficult to visualise the
appendix but adjacent to the caecum a 10mm low attenuation lesion
with mural calcification was noted suggestive of an appendicular
mucocele. No pelvic or retroperitoneal lymphadenopathy was noted
and no lesions were noted within the chest.
Figure 2 Histology of the appendix tip showed mucinous material within
the bowel wall and stroma suggesting a mucocele or mucinous tumour of the
appendix.
Figure 3: The patient underwent a right hemicolectomy during
which further endometriotic deposits were seen. The appendix
appeared abnormal as it was thickened and adherent to caecum with
mucinous material extruding from the tip. Three proximal puckered
lesions were noted in last 20cm of the terminal ileum but no other
peritoneal disease was noted.
Histological results found the same appendix showed.
i) Mucinous cystadenoma of the appendix
ii) Well differentiated carcinoid tumour measuring 10mm in diameter
iii) Coexistent features of endometriosis
Figure 4 & Figure 5: Currently, the patient is well and conceived
naturally whilst waiting to start IVF treatment.
Figure 3 CT scan. Adjacent to the caecum a 10mm low attenuation lesion
with mural calcification was noted suggestive of an appendicular mucocele.
Figure 4 Appendis take from hemicolectomy specimen, showing mucin on
the serosal surface.
Figure 5 Nests of carcinoid tumour cells (red arrow) infiltrating appendiceal wall.
Combined mucinous cystadenoma and carcinoid tumour of the appendix with coexistent features of an
endometrioma: a case report
7
Copyright:
©2014 Dunkerton et al.
Citation: Dunkerton S, Pankhania NK, Johnson C, et al. Combined mucinous cystadenoma and carcinoid tumour of the appendix with coexistent features of
an endometrioma: a case report. Obstet Gynecol Int J . 2014;1(1):5‒7. DOI: 10.15406/ogij.2014.01.00001
Discussion
Endometriosis is one of the most common diseases seen by
gynaecologists. The prevalence is difficult to estimate as women can
be asymptomatic or present with varying degrees of pelvic pain. 11
Endometriosis is associated with infertility and has been identified
in 38.5% of infertile women as opposed to 5.2% of fertile women.12
Appendicular tumours have diverse histology. Carcinoid neoplasms
are the most common, accounting for 66% of all tumours of the
appendix. They are comprised of enterochromaffin cells and contain
many neurosecretory granules that release serotonin, histamine and
prostaglandins.13 As with endometriosis, the incidence and prevalence
is unknown, as the disease is mainly asymptomatic. The average time
for a carcinoid tumour to become symptomatic is 9 years. Carcinoid
tumours may present late and be associated with metastasis if found
within the tip of the appendix.
The most common benign appendix tumours are mucinous
cystadenomas. These tumours are composed of intestinal epithelium
are dysplastic and secrete mucin, giving rise to a mucocele. This often
causes the appendix to dilate and can present as acute appendicitis. The
presence of a mucinous cystadenoma with associated mucin within
the appendix wall increases the risk of psuedomyxoma peritonei.
There have been reports in literature of the co-existence of two
types of appendicular tumours. Alsaad et al. 14 reported a case of
combined goblet cell carcinoid and mucinous cyst-adenoma of the
appendix in a patient presenting with right iliac fossa pain. The
occurrence of appendicular tumours co-existing with endometriosis
is rarely reported, 15 and there have been no reported cases of two
different appendicular tumours being found with co-existent features
of an endometrioma within the same appendix. Appendicectomy
specimens should be routinely sent for histopathological analysis.
Duzgan et al.15 reported an intra-operative detection rate of less than
50% for all types of appendicular tumours. Jones et al (2007) evaluated
the histopathological reports of 1225 appendicectomy specimens. Of
the 1225, 46 (3.75%) revealed abnormal diagnoses and 24 (1.96%)
were clinically significant, altering patient management. 16 Routine
histopathological analysis avoids the potential to miss significant
pathologies which may need different treatments.
Currently in the literature there are no clear guidelines regarding
the treatment of appendicular tumours.17 There is considerable debate
as to the use of appendectomy versus right hemicolectomy and the
effects on long term results. A right hemicolectomy is indicated
with adenocarcinomas, tumours invading the mesoappendix, serosa,
lymphatics or vasculature and benign tumours with a diameter
of more than 2cm. 18 As preferred by some surgical units 19 a right
hemicolectomy is considered the treatment of choice. There was
suspicion of a malignant adenocarcinoma after initial biopsy which
rendered a right hemicolectomy a safer option.
Conclusion
Most surgeons will only encounter a few carcinoid tumours of
the appendix in their career. We feel this unique case will add to the
small database of similar reports and help with management of this
rare disease.
This case illustrates the broad spectrum of appendicular and
endometriotic disease. It also demonstrates the role of biopsy of
abnormal areas atypical of endometriosis at diagnostic laparoscopy.
We hope to highlight the interesting asymptomatic presentation
of this patient and therefore the importance of requesting routine
histopathological analysis. After prompt treatment with right
hemicolectomy, this young woman has fortunately conceived
naturally without IVF.
Acknowledgments
None.
Conflicts of interest
Author has no any conflict of interest to declare.
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