Vaginal Reconstruction for Vaginal Obliteration Secondary to Stevens Johnson Syndrome: A Case Report and Review of Literature.

Vulvovaginal involvement is as common as 70% during the acute phase of SJS.7 The most frequently detected genital lesions are erosive and ulcerative vaginitis and vulvar bullae. These lesions tend to resolve in 1–8 weeks, but they may persist for several months and up to a year following the acute period of the disease. Long-term consequences of genital involvement are labial agglutination, introital stenosis, vaginal synechiae and stenosis, vaginal and vulval adenosis, hematocolpos, and hematometra. Endometriosis may occur due to scarring in up to 28% of patients.8,9 The main complaints secondary to these long-term complications are dryness, itching, burning sensation, post-coital bleeding, dyspareunia, or the inability to have sexual intercourse.9 Nevertheless, complete vaginal obliteration is rare according to the review of the published literature. In the largest series published on this issue, Meneux et al,7 reported that although genital lesions are common during the acute phase of the disease, sequelae occurred in only five of 40 patients (12.5%). In that group, two of the five women had surgical correction with long-term genital consequences. Among those, one had a recurrence six months post-surgery, and the other had no recurrence, but she was unable to have sexual intercourse.7 Graham-Brown et al,10 reported another case who developed hematocolpos due to complete vaginal stenosis following SJS in pregnancy. Wilson et al,11 described a case with severe vaginal stenosis who underwent a successful surgical correction. Hart et al,12 reported vaginoscopic division of vaginal adhesions for an 11-year-old girl after recovery from the systemic phase of SJS and they recommended that all patients with SJS with vaginal involvement undergo routine follow-up to evaluate and treat vaginal adhesions. In another report, a girl who developed SJS as a child experienced hematometra after the onset of puberty, and she required surgery to treat genital adhesions.13 Murphy and Brant,14 published a case with severe vaginal adhesions that led to the fusion of introitus. The patient was a 14-year-old girl who presented with lower abdominal pain and amenorrhea that persisted for five months. She was diagnosed with hematocolpos secondary to SJS and underwent surgery for fused introitus.14 Similarly, a 10-year-old girl with a history of SJS at age 4 was diagnosed with hydrometrocolpos secondary to extensive labial synechiae that completely covered the clitoris, urethral meatus, and vaginal opening. She required surgical reconstruction.15 Madhuri et al,16 reported a 32-year-old patient with a history of SJS who underwent excision of a single thick adhesion across the entire upper-third of the vagina. In our patient, we detected complete synechiae of the distal vagina beginning at the level of the introitus. Since she was amenorrheic for the last three years due to the levonorgestrel-releasing IUD, hematocolpos, and hematometra did not develop. Additionally, she did not report coital problems because she was not sexually active. Her family physician incidentally diagnosed vaginal obliteration after a failed attempt to remove her IUD. Otherwise, she did not report any genital complaints. The surgery revealed that she had pyocolpos occupying the upper half of the vagina. Her vaginal synechiae was so firm that separation of the fused vaginal walls either with blunt or sharp dissection was impossible. Therefore, rectovaginal space dissection became inevitable to treat the obstruction. For female patients with SJS, genital examination should be scheduled as early as possible to avoid genital tract obstruction and future sexual problems.15 This is especially mandatory in patients who report vaginal discomfort or discharge since these complaints indicate the presence of vaginal erosion and ulceration. In this situation, early identification may be possible, and early management may prevent the development of vulvovaginal adhesions and associated subsequent complications.16 Placing a soft mold in the vagina with the use of local corticosteroids until resolution of the acute phase of illness may be considered to prevent adhesions.8 However, such an approach poses a risk of infection and sepsis in the acute phase due to systemic absorption of topical steroids.9 Instead, a lubricant gel can be applied to lesions in the acute phase to prevent adhesions. Also, sexual intercourse immediately after the acute phase following wound epithelization was proposed by some authors to help reduce stenosis, but most patients may reject this.6,8 When fine adhesions are detected early in the course of SJS, the division of these adhesions as a relatively minor procedure may be helpful in preventing the development of thick fibrous bands and severe sequelae such as introital stenosis, vaginal narrowing, or complete vaginal canal obliteration.14 Gynecology consultation was not scheduled for our patient during or immediately after the acute phase of SJS. This might have contributed to her significant vaginal sequelae, which was detected incidentally since she was sexually inactive and amenorrheic.

Genital involvement is frequent in the acute phase of SJS, but long-term consequences are not so uncommon and symptomatic genital tract obstruction is rarely seen. On the other hand, such an obstruction usually necessitates major surgical procedures. The review of the literature showed only eight cases who required surgery for long-term genital sequelae. Therefore, the gynecologists should examine women with SJS as early as possible during the acute phase of condition since preventive measures are available that may help reduce the risk of severe long-term sequelae. Disclosure The authors declared no conflicts of interest.

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