Metastatic Spread of Mucinous Cystadenocarcinoma of The Ovaries Into Abdominal Wall

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Metastatic spread of mucinous cystadenocarcinoma of the


ovaries into abdominal wall
Dragan iki, Aljoa Mandi, Marina Popovi, Katarina Koprivek, Milana Panjkovi
ABSTRACT
Epithelial ovarian cancer belongs to the most common and most deadly of all types of ovarian carcino-
mas. Ovarian cancer affects women in the age group 65 years and older more frequently than younger
women. Approximately 75% of cases will have spread beyond the ovaries at the time of diagnosis.
Twenty-two year old patient was treated at the Institute of Oncology Sremska Kamenica, in the period
from 1998 until 2000. In 1993, she underwent left salphingo-oopherectomy; histopathological finding
was mucinous cystadenoma of the ovaries. In 1994, mucinous papillary cystadenoma with borderline
malignancy confirmed by histopathological findings was found after abdominal hysterectomy with right
salpingo-oopherectomy and total omentectomy. The patient was well until 1998 when she palpated a
tumor mass in the front abdominal wall with pain in that region. Tumor was extirpated and final
histopathological finding was mucinous adenocarcinoma in fibrous tissue. The patient received with
chemotherapy (carboplatin and cyclophosphamide) and external-beam radiotherapy. Recurrence free
survival rate was 20 months but in April 2000, patient came back with recurrence of the disease. It was
the same spread into abdominal wall. Rectus abdominis muscle was resected and plastic surgery of
abdominal wall was performed. After operation patient received second line chemotherapy according to
the same protocol. However, during the treatment the disease spread into abdominal cavity and affect-
ed small intestine and liver.
KEY WORDS: Cystadenocarcinoma, Mucinous; Ovarian Neoplasms; Neoplasm Metastasis; Abdominal
Wall
Institute of Oncology Sremska Kamenica, Serbia &
Montenegro; Address correspondence to: Dr. Dragan iki,
Institute of Oncology Sremska Kamenica, Institutski put 4,
21204 Sremska Kamenica, Serbia & Montenegro, E-mail:
[email protected]; The manuscript was received:
08.07.2005, Provisionally acepted: 11.07.2005, Accepted
for publication: 15.07.2005
2005, Institute of Oncology Sremska Kamenica, Serbia &
Montenegro
Arch Oncol 2005;13(2):86-8.
DOI: 10.2298/AOO0502086Z
CASE REPORT
UDC: 618.11-006:616-089.8
INTRODUCTION
I
n the past decade, the number of ovarian cancers has increased 30% and the number of
ovarian cancer deaths has increased 18% (1). In 1990, ovarian cancer was the fourth
most common cancer in women and the most common gynecological cancer, with 29,353
new cases in the European Union. It was the fifth most common cause of cancer death
(22,166 deaths)(2). In 1999, ovarian cancer was the second most frequent gynecological
cancer in Western Europe, causing around 82,000 deaths (3). Morbidity and mortality of
ovarian cancer shows an average increase in the Republic of Serbia, which points to the
importance of early diagnostic procedures and looking for the best options for screening
program in women population (4,5). Ovarian cancer is primarily a disease of post-
menopausal women, the highest number of cases being concentrated in the age group from
50 to 70 years (6,7). Because of the position of the ovaries deep within the abdomen ovar-
ian cancer is often asymptomatic in its early stages, most patients have a widespread dis-
ease at the time of diagnosis (8). Approximately in 75% of cases will have spread beyond
the ovaries at the time of diagnosis (9). Surgery is required for a full diagnosis and also rep-
resents the main form of treatment for early-stage disease, which is confined to the ovaries.
The purpose of surgery is to establish or confirm the suspected diagnosis; to surgically
stage the patient with apparent early-stage disease; and in the event of advanced-stage dis-
ease, to remove as much tumor mass as possible. However, for patients who present with
advanced stage III and IV disease, where the tumor has spread beyond the pelvic region into
the abdominal cavity and/or distant sites, the initial surgical treatment is followed by
chemotherapy. Ovarian tumors are sensitive to chemotherapy, and most stage III and IV
patients receive chemotherapy to increase their survival and improve their quality of life
(QoL) (9-12).
A CASE REPORT
A young 22-year old patient with ovarian epithelial cancer was treated at the Institute of
Oncology Sremska Kamenica, from 1998 to 2000. Final histopathological finding was
mucinous cystadenocarcinoma of the ovaries. International Federation of Obstetricians and
Gynecologists (FIGO) classification was used for disease staging.
According to the gynecological anamnesis patient was virgin, her menarche occurred when
she was 13 years old and menstrual cycles were orderly. No hereditary factors or any other
risk factors for ovarian cancer were found in family anamnesis. She was operated in 1993
and left salphingo-oopherectomy was performed. Histopathological finding was mucinous
cystadenoma of the ovaries. One year later (1994), there were some changes at the right
ovary, which were found during the routine transvaginal ultrasonography control. There was
not any clinical symptom and there was no data about serum level of CA125. Abdominal
hysterectomy with right salpingo-oopherectomy and total omentectomy was performed.
Final histopathological result was ovarian tumor: mucinous papillary cystadenocarcinoma
with borderline malignancy. The patient was regularly checked up during next few years;
she had no clinical symptoms of the disease and her Karnofsky score was 100. In 1998,
www.onk.ns.ac.yu/Archive July 30, 2005
she palpated a tumor mass in the front abdominal wall with pain in that region. The whole
tumor node was extirpated and final histopathological finding was mucinous adenocarcino-
ma in fibrous tissue. Cytological examination of the lavage of the abdominal cavity was
without malignancy.
The patient received four cycles of chemotherapy according to the protocol: carboplatin
(300mg/m
2
) and cyclophosphamide (600mg/m
2
) every three weeks. Side effects were
controlled for hemopoietic system and function of liver and kidneys one week after therapy
application and one week before next cycle of chemotherapy. During the first two cycles,
she received external-beam radiotherapy, 30 Gy in 30 daily fractions. After six cycles of
chemotherapy and radiotherapy patient felt well and had no clinical symptoms. Recurrence
free survival rate was 20 months.
In April 2000, the patient came to the Institute complaining with pain and pressure in right
side of the front abdominal wall and tumor, which was painful during clinical exam. Nuclear
magnetic resonance was performed which confirmed tumor infiltration in the abdominal
wall (Figure 1,2).
Musculus rectus abdomini was resected and plastic surgery of abdominal wall was per-
formed. There was no ascites and during operation two metastatic nodes less than 3 mm
in diameter were found in small intestine. Material from the scarring tissue, serosal surface
of the small intestine, part of the striate muscle, and the other structures of the anterior
abdominal wall were sent for pathology examination. On the microscopic examination a tis-
sue of adenocarcinoma was found in the structures of the anterior wall: fibrous, adipose tis-
sue and striate muscle, as well as on the serosal surface and the wall of the small intestine
without extending through the mucosa. Tumor tissue was composed of well-differentiated
glandular structures with the small production of the mucin and the areas of necrosis.
The patient was indicated for second-line chemotherapy with carboplatin (300mg/m
2
) and
cyclophosphamide (600mg/m
2
), six series, every three weeks. During the cycle 5, the
patient experienced abdominal pain, obstipation, lost of appetite, fatigue, and anemia.
Computer tomography was performed which showed widespread metastases in small
intestine and liver.
The cycle 6 of chemotherapy was not administered and the patient received symptomatic
therapy. She died in December 2000.
DISCUSSION
Ovarian cancer is one of the biggest problems in gynecologic oncology. Because of diffi-
cult to diagnose at an early stage most are diagnosed at an advanced stage. Early detec-
tion requires a reliable screening test. An optimal screening test has high sensitivity, speci-
ficity, and patient acceptance, and is easy to perform. The three screening techniques avail-
able at this time (pelvic examination, CA-125 level, and vaginal ultrasound) do not actually
diagnose ovarian cancer but only suggest its presence.
As with many cancers, advancing age is the most significant risk factor for the development
of ovarian cancer. Marchetti M et al. showed in that of 545 patients with epithelial ovarian
cancer 49 were under 35 year old and mostly histopathological findings in that group of
patients was borderline tumor and ovarian cancer in early-stage of the disease that
increased 5-year survival rate. This showed that advancing age could be, besides as risk
factor, important prognostic factor (13).
Pelvic masses found in women of reproductive and postmenopausal age must be evaluat-
ed preoperatively to determine the probability of malignancy. A pelvic mass in a woman of
reproductive age may be a functional cyst, particularly if the mass is cystic, less than 6 to
8 centimeters in diameter, unilateral, and mobile. If all of these criteria are present, it is
appropriate to reexamine the patient in four to six weeks. If the mass persists or has grown,
exploratory laparotomy or laparoscopy is indicated. A woman with a solid or partially cys-
tic mass, ascites, and/or an elevated CA-125 level should be operated on by a gynecolog-
ic oncologist or by a surgical team with the necessary skills to surgically stage or debulk
the disease. All surgeons who attend women with suspected ovarian malignancy must
understand importance of performing appropriate surgical staging and debulking of ovarian
cancer. Ovarian cancer is a surgically staged disease. In apparent early-stage disease,
complete surgical staging is critical for the selection of adjunctive therapy. In advanced-
stage disease, the goal is primary cytoreduction (14).
A literature review showed that patients with optimal cytoreduction had median survival of
39 months compared with survival of only 17 months in patients with suboptimal surgery
(15). However, results of a retrospective analysis of 349 patients with postoperative resid-
ual masses less than or equal to 1 centimeter suggest that patients who present with large-
volume disease and achieve small-volume disease by surgical debulking have poorer out-
comes than similar patients who present with small-volume disease (16). Standard post-
operative therapy for advanced-stage ovarian cancer includes platinum-based chemother-
apy with the substitution of paclitaxel for cyclophosphamide (12,17,18).
Ovarian cancer usually spreads via local spreading into the peritoneal cavity followed by
attachment to the peritoneum, and via local invasion into the bowel and bladder. This kind
of tumor rarely spreads out of abdominal cavity; in our case the main localization of
metastatic spread was in abdominal wall for two times before tumor spread into the liver.
The incidence of positive nodes at primary surgery has been reported as high as 24% in
patients with stage I disease, 50% in patient with stage II disease, 74% in patients with stage
III disease, and 73% in patients with stage IV disease (19).
Metastatic spread of mucinous cystoadenocarcinoma
87
www.onk.ns.ac.yu/Archive July 30, 2005
Figure 1. Transverse T2W spin echo image demonstrates heterogeneous, high signal intensity mass
in the right rectus abdominis muscle, without distinctive borders to the surrounding structures of the
anterior abdominal wall. There is no evidence of peritoneal based metastases
Figure 2. Transverse T1W spin echo image reveals only an enlargement of the rectus abdominis on
the right side. The conspicuity of the tumor is reduced, due to the similar signal characteristics of both
the tumor and adjacent muscle
Abdominal wall metastases of ovarian cancer are very rare but not impossible (20,21).
They represent more or less 1% of human neoplasms in the adult. Abdominal wall neo-
plasm are less aggressive for compartmentalization of muscle layer and with a better prog-
nosis because of their localization, and surgical opportunities of extensive resection (not
less of 2 cm from tumor's macroscopic limits) allowed by modern prosthetic reconstruc-
tion techniques (22). Abdominal wall metastases can also occur after laparoscopic proce-
dure in treatment of gynecologic neoplasms (23,24).
An inadequate surgical management performed by laparoscopy and laparotomy may wors-
en the prognosis of an early ovarian cancer. If the abdominal wall is protected with a bag
and the tumor is not morcellated, the incidence of trocar site metastasis is about 1%.
Puncture of an ovarian tumor with intracystic vegetations is a high-risk situation which
should be avoided whenever possible (25).
CONCLUSION
Ovarian cancer is difficult to diagnose at an early stage. Thus, most are at an advanced
stage when discovered. Histopathological confirmation of the disease, surgical staging, and
aggressive surgical debulking, when possible, are all part of the initial evaluation and treat-
ment of ovarian cancer. In most cases, surgery is followed by chemotherapy. Advancing
age, the major risk factor for the development of ovarian cancer is, of course, unalterable.
The patient treated in the Institute of Oncology Sremska Kamenica was 22 year old and
metastasis appeared in abdominal wall 4 years after borderline tumor of ovary had been
diagnosed. Recurrence free survival rate was 20 months.
REFERENCES
1. Wingo PA, Tong T, Bolden S. Cancer statistics, 1995. CA Cancer J Clin 1995;45:8-30.
2. Black RF, Bray F, Ferlay J. Cancer incidence and mortality in the European Union: cancer registry
data and estimates of national incidence for 1990. Eur J Cancer 1997;33:1075-107.
3. Piccart MJ, du Bois A, Gore ME. A new standard care for treatment of ovarian cancer. Eur J
Cancer 2000;36:10-2.
4. Markovic-Deni Lj, ivkovic S, Rakoevi I. Epidemiologija malignih bolesti enskih genitalnih
organa u centralnoj Srbiji; Zbornik radova XLV Ginekoloko-akuerska nedelja; 2001:153-8.
5. Jevremovi I, Jankovi S, Gledovi Z. Smrtnost od najeih malignih tumora ena u Srbiji.
Vojnosanit Pregl 1994;51:114-7.
6. Pecorelli S, Odicino F, Maisonneuve P. Carcinoma of the ovary. J Epidemiol Biostats 1998;3:75-102.
7. Rubin S, Fennelly D, Randall ME. Ovarian cancer. In: Pazdur R, Coia L, Wagman L, Hoskins W,
editors. Cancer management: a multidisciplinary approach. Huntington, NY: PRR Inc.; 1996. p.
185-205.
8. Mandi A, Tei M, Vujkov T, Novta N, Rajovi J. Ovarian cancer stage III/IV: poor prognostic
factors. Arch Oncol 2001;9(1):169-70.
9. Young RC, Perez CA, Hoskins WJ. Cancer of the ovary. In: DeVita VT Jr, Hellman S, Rosenberg
SA, editors. Cancer: Principles and Practice of Oncology. 4th ed. Philadelphia, PA: JB Lippincott
Co; 1993. p. 1226-63.
10. McGuire WP, Hoskins WJ, Brady MD. Cyclophosphamide and cisplatin compared with paclitaxel
and cisplatin in patients with stage III and stage IV ovarian cancer. N Engl J Med 1996;334:1-6.
11. Sandercoc J, Parmar MK, Torri V. First-line chemotherapy for advanced ovarian cancer: pacli-
taxel,cisplatin and the evidence. Br J Cancer 1998;78:1471-8.
12. Piccart MJ, Bertelsen K, James K, Cassidy J, Mangioni C, Simonsen E, et al. Randomized inter-
group trial of cisplatin-paclitaxel versus cisplatin-cyclophosphamide in women with advanced
epithelial ovarian cancer: three-year results. J Natl Cancer Inst 2000;92(9):699-708.
13. Marchetti M, Chiarelli S, Silvestri P, Peron ML. Epithelial ovarian tumors in young women under
35 years. Eur J Gynaecol Oncol 1995;16(6):488-93.
14. Edward E, Partridge MD, Mack N, Barnes MD. Epithelial Ovarian Cancer: Prevention, Diagnosis,
and Treatment. CA Cancer J Clin 1999;49:297-320.
15. Hoskins WJ. Surgical staging and cytoreductive surgery of epithelial ovarian cancer. Cancer
1993;71(4 Suppl):1534-40.
16. Hoskins WJ, Bundy BN, Thigpen JT. The influence of cytoreductive surgery on recurrence-free
interval and survival in small-volume stage III epithelial ovarian cancer:a Gynecologic Oncology
Group study. Gynecologic Oncology 1992;47(2):159-66.
17. Piccart MJ, du Bois A, Gore ME. A new standard care for treatment of ovarian cancer. Eur J
Cancer 2000;36:10-2.
18. Neijt JP, Engelholm SA, Tuxen MK. Exploratory phase III study of paclitaxel and cisplatin versus
paclitaxel and carboplatin in advanced ovarian cancer. J Clin Oncol 2000;18:3084-92.
19. Burghard E, Brady MF, Homesley HD. Patterns of pelvic and paraarortic lymp node involvement
in ovarian cancer. Gynecol Oncol 1991;40(2):103-6.
20. Haughney RV, Slade RJ, Brain AN. An isolated abdominal wall metastasis of ovarian carcinoma
ten years after primary surgery. Eur J Gynaecol Oncol 2001;22(2):102-3.
21. Baron MA, Ladonne JM, Resch B. Abdominal wall metastasis from ovarian cancer after laparo-
tomy. A case report. Eur J Gynaecol Oncol 2002;23(6):561-2.
22. Donati M, Gandolfo L, Brancato G, Caglia P, Cavallaro G, D'Addea I, et al. Surgical tactics in
abdominal wall neoplasia.Tumori 2003;89(4 Suppl):61-2.
23. van Dam PA, De Cloedt J, Tjalma WA, Buytaert P, Becquart D, Vergote IB. Trocar implantation
metastasis after laparoscopy in patients with advanced ovarian cancer: can the risk be reduced?
Am J Obstet Gynecol 1999;181(3):536-41.
24. Picone O, Aucouturier JS, Louboutin A, Coscas Y, Camus E. Abdominal wall metastasis of a cer-
vical adenocarcinoma at the laparoscopic trocar insertion site after ovarian transposition: case
report and review of the literature. Gynecol Oncol 2003;90(2):446-9.
25. Canis M, Mage G, Botchorishvili R, Wattiez A, Rabischong B, Houlle C, et al. Laparoscopy and
gynecologic cancer: is it still necessary to debate or only convince the incredulous? Gynecol
Obstet Fertil 2001;29(12):913-8.
iki D. et al.
88
www.onk.ns.ac.yu/Archive July 30, 2005

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