Abstract
Gynecological fistulas that are familiar are vesicovaginal, rectovaginal and
ureterovaginal fistulas, which may be due to childbirth, operative injury, tumour or
radiation. Tubocutaneous fistula, is as a very rare condition secondary to tuberculosis,
endometriosis, and complications of child birth and gynecological surgeries. We
report a 30 year old woman with a tuberculous tubocutaneous fistula, arising from
the right salphingeal tube and discharging in the lower abdomen cutaneously, who
underwent laparoscopic right salpingo oophorectomy, and excision of the tract upto
the skin, and the abdominal wall, with open excision of the distal part. The case is
being published for its rarity, and to remind gynecologists to consider this possibility
in a non-healing sinus in the lower abdomen. The authors believe this to be the first
such case in literature.
Obstetrics & Gynecology International Journal
Case Report
Open Access
Laparoscopic Excision of Tubocutaneous Fistula: Case Report
420
Copyright:
©2018 Rajkumar et al.
Citation: Rajkumar JS, Ganesh D, Syed A, et al. Laparoscopic Excision of T ubocutaneous Fistula: Case Report. Obstet Gynecol Int J. 2018;9(6):419‒421.
DOI: 10.15406/ogij.2018.09.00378
negligible. Closure was done in layers after washing out the abdominal
wall thoroughly. The specimen was sent for histopathology.
Figure 3a Medial part of dissection of the tube, inflammatory mass and the
tract going upto the anterior abdominal wall.
Figure 3b Dissection of distal portion of ovary, inflammatory mass and the
tract upto anterior abdominal wall.
Figure 4 Excision of Fistulous tract.
Post-operatively, the patient was put on antibiotics and analgesics.
She had no infection of the wound and was back to normal in a few days.
Histopathology revealed simple serous ovarian cyst with fistulous tract
running from the inner lining of the right fallopian tube up to the skin,
and this was surrounded by granulation tissue with epithelioid cells,
Langhans giant cells, lymphocytes, highly suggestive of tuberculosis.
Pus cultures were negative for growth of mycobacterium, but the PCR
of the fluid was positive for Mycobacterium tuberculosis. The patient
was subsequently started on anti-tuberculous therapy, and at follow
up was asymptomatic.
Figure 5 Final appearance.
Discussion
Wittich et al in 1982 first reported a tubocutaneous fistula. 1 This
case on retrospect is a tuberculous tuboctaneous fistula, commencing
in a tuberculous tubo- ovarian abscess, and finding its way to the skin.
Is it a fistula?
Yes, because both epithelial surfaces were clearly connected, the
tubal and the cutaneous.
Where did the infection begin?
Tubo- ovarian tuberculosis is well known, although its presentation
as a fistula is extremely rare.
A pathological communication between the fallopian tube and skin
is quite rare. Causes described in literature are pelvic inflammatory
disease, Crohn’s disease, tuberculosis, endometriosis, inflammatory
bowel disease and pelvic surgeries.2–5 The current literature advocates
salpingectomy or salpingo-oophorectomy and complete excision
of the tract as definitive treatment. 6 Nayini et al reported a case
without any specific disease process. The best imaging modality
recommended is MRI or CT scan. 7 A high index of suspicion in a
persistently discharging sinus of the lower abdomen is required. Belli
et al reported a persistent ischiorectal fistula of tubo-ovarian origin.8
All the available reports, intra-operative details are of open surgery
only.2–11 In our case, we used the ‘medial to lateral’ approach. As the
medial end of the fallopian tube and broad ligament were unaffected
in the inflammatory process, we disconnected the medial attachments
first. The next step was to devascularise the inflammatory phlegmon
completely, and the ovarian vessels were sealed and cut. The rest
of the dissection consisted of removing the entire fistula up to the
peritoneum. Perhaps a PCR testing in the early stages of her disease
might have yielded results for aggressive antitubercular therapy.
A small number of cases have been reported of fistulas between the
fallopian tube and the neighbouring colon, small bowel, or bladder, all
these fistulas managed by laparotomies. To our knowledge, this is the
first ever case report of a Total Laparoscopic excision of a tuberculous
tubocutaneous fistula.
Conclusion
This article highlights the need to consider the possibility of an
underlying Tubocutaneous or Uterocutaneous fistula as a cause
Laparoscopic Excision of Tubocutaneous Fistula: Case Report
421
Copyright:
©2018 Rajkumar et al.
Citation: Rajkumar JS, Ganesh D, Syed A, et al. Laparoscopic Excision of T ubocutaneous Fistula: Case Report. Obstet Gynecol Int J. 2018;9(6):419‒421.
DOI: 10.15406/ogij.2018.09.00378
for a non-healing lower abdominal sinus, especially after multiple
explorations. Early diagnosis and adequate surgical clearance will
serve to prevent complications in the long term. This case, a Totally
Laparoscopic excision of a Tubocutaneous Tuberculous fistula,
is being published, as it is the first of its kind in literature, to our
knowledge.
Acknowledgments
None.
Conflict of interest
The authors declare that they have no conflict of interest.
References
1. Wittich AC, Morales H, Braeuer NR. Tubocutaneous fistula. Am J Obstet
Gynecol. 1982;144(1):109–110.
2. Shukla D, Pandey S, Pandey LK, et al. Repair of uterocutaneous fistula.
Obstet Gynecol. 2006;108(3 Pt 2):732–733.
3. Ogbeide OU, Ukadike IA, Ehigiamusoe FO, et al. Acquired salpingo-
enteric fistula—a case report. Afr J Reprod Health. 2010;14(1):139–143.
4. Abasiattai AM, Ibanga GJ, Akpan A, et al. Post caesarean section
uterocutaneous fistula: a case report. Women’ s Health, Issues & Care.
2014;3(5).
5. Sheikh MA, Begum J, Balasubramanian G. Tuboenterocutaneous fistula
following caesarean section. International J Reproduction Contraception,
Obstetrics & Gynecology. 2014;3(1).
6. Palnaes-Hansen C, Bülow S, Karlsen J. Tubocutaneous fistula,Case
report. Acta Chir Scand. 1987;153(7–8):465–466.
7. Krishnaveni Nayini, Clive Gie. Tubocutaneous fistula a case report. Case
Reports in Obstetrics & Gynecology. 2015.
8. Belli EV , Landmann RG, Koonce SL, et al. Persistent ischiorectal fistula
with supralevator origin secondary to a chronic tubo-ovarian abscess:
report of a case and review of the literature. Female Pelvic Med Reconstr
Surg. 2012;18(1):66–67.
9. Lopes EN, Dam ásio LC, Passos LS. Tubocutaneous fistula due to
endometriosis-a differential diagnosis in cutaneous fistulas with cyclic
secretion. Rev Bras Ginecol Obstet. 2017;39(1):31–34.
10. Choe SA, Lee HJ, Moon KY , et al. A tubocutaneous fistula in a patient
with Chro’s disease after multiple laparotomies: a case report. J of
Women’ s Med. 2008;1(2);188–189.
11. London AM, Burkman RT. Tuboovarian abscess with associated rupture
and fistula formation into the urinary bladder: report of two cases. Am J
Obstet Gynecol. 1979;135(8):1113–1114.
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