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ّ̃ᗕࡪࡩ۞Ғ৵ε༰াЪ׀ າϠಏ৷ ৃঽ߲ຏߖ ࣫ܫඕ ᆒڌ လӖ ̋̚ᗁጯ̂ጯܢనᗁੰϩቲࡊ Female Twins with Incontinentia Pigmenti and Concurrent Neonatal Herpes Simplex Virus Infection Hsin-Chieh Tang Tun-Yuan Liu Chia-Chun Kao Rows of vesicles over erythematous bases are the typical cutaneous lesions of the first stage of incontinentia pigmenti (IP). But the clinical lesions share the same features with herpetic vesicles. We present a couple of female twins with generalized vesicular eruptions over the trunk and limbs at birth. The pathologic findings were consistent with first stage IP. In addition, an isolated group of vesicles was noted at the vertex of the scalp. Pathologic examination and viral culture proved herpes simplex virus ( HSV ) infection. Ophtholmologic examination demonstrated retinopathy which consisted of venous engorgement and soft exudates on the retina. Viral cultures of the eyes were positive for herpes virus. Because the course or management of IP and HSV infection is quite different, we suggest that both of the diseases need to be considered in the differential diagnosis of neonatal blistering disorders. (Dermatol Sinica 21 : 293-297, 2003) Key words: Incontinentia pigmenti, Herpes simplex virus ௐ˘ഇҒ৵ε༰া۞ݭϩቲᓜԖܑனߏ˘ፋଵ۞ͪڽΐ˯ࡓҒ۞ૄغĄҭߏ ৃঽ ߲ԛј۞ͪົ˵ڽѣ࠹Т۞ᓜԖܑனĄԧࣇಡӘ˘၆ّ̃ᗕࡪࡩдϠॡ֗វᄃα۳ன ᇃ̶ڽͪ۞ّھοĄঽந̷ͯ۞ඕߏڍЪௐ˘ഇҒ৵ε༰া۞෧ᕝĄੵѩ̝γĂдсࣇ ۞ᐝ˯൴ன˘ཏϲ۞ͪڽĄঽந̷ͯᄃঽ߲ૈዳᙋ၁˞ࠎಏ৷ ৃঽ߲۞ຏߖĄீ ࡊ۞ᑭߤ൴னѣෛშቯᐖਔᕖૺᄃహّႣ୵۞ෛშቯঽតĄீ༗۞ঽ߲ૈዳܜ˞ ৃঽ߲ĄЯࠎҒ৵ε༰াᄃಏ৷ ৃঽ߲ຏߖ۞ঽந͞ёၟ̙ТĂԧࣇޙᛉ ়ঽᅮࢋЕˢາϠڽͪঽ۞ᝥҾ෧ᕝĄ(̚රϩᄫ21 : 293 - 297, 2003) From the Department of Dermatology, Chung Shan Medical University Hospital Accepted for publication: March, 28, 2003 Reprint requests: Department of Dermatology, Hsin-chieh Tang, M.D., No. 110, Sec. 1, Jianguo N. Rd., Taichung, Taiwan TEL: 886-4-24739595 ext. 2338 293 ّ̃ᗕࡪࡩ۞Ғ৵ε༰াЪ׀າϠಏ৷ ৃঽ߲ຏߖ INTRODUCTION Incontinentia pigmenti (IP) is an X-linked dominantly inherited disease with characteristic skin lesions and stages. Females are mainly affected, and males who got the abnormal gene are usually lethal.1, 2 Linear rows of vesicles over erythematous bases mainly on the extremities and occasionally on the trunk are the typical cutaneous lesions of the first stage of IP. But the clinical lesions share the same features with herpetic vesicles. Because neonatal herpes simplex virus ( HSV ) infection has the prevalence of 1 in 2000 live births, and it may produce severe complications that complicate the management of infants with IP, we should keep in mind that the possibility of these two diseases may occur in the same patient.3, 4, 5, 6 CASE REPORT The twins were female newborns born by vaginal delivery to a gravida 4 para 4 ( G4P4 ) mother without abortion history. The mother did not receive any prenatal screens, and she denied any congenital disease or sexual transmitted disease. Generalized vesicular eruptions over the trunk and limbs of the twins were present at birth. Physical examination revealed that some rice-grain to bean-sized vesicles lying over erythematous bases appeared in a linear distribution on the trunk and limbs (Fig. 1A). The face and neck were not involved. An isolated group of vesicles was noted at the vertex of the scalp since the day of 7 and 8 ( twin A and twin B, respectively ) ( Fig. 2A ). Laboratory data showed leukocytosis (WBC: 13200 and 14500, Fig. 1 Fig. 2 (A) Some vesicles lying over erythematous bases appeared in a linear distribution on the trunk (twin A). (B) This field revealed eosinophilic spongiosis, individual necrotic keratinocytes, and infiltration of eosinophils in the dermis. (H & E, x200) (A) An isolated group of vesicles was noted at the vertex of the scalp (twin A). (B) This field showed multinucleated giant cells and balloon cells around the keratinocytes. (H & E, x400) Dermatol Sinica, September 2003 294 ࣫ܫඕ respectively ) and eosinophilia ( Eosinophils count: 24 % and 25 %, respectively ). Maternal herpes antibody IgM was positive but IgG was negative. The newborns' herpes antibody IgM and IgG were negative. Pathologic examination of skin biopsy from the vesicles located on the trunk and legs of the twins revealed eosinophilic spongiosis. Individual necrotic keratinocytes were present within the epidermis. Besides, eosinophils also infiltrate in the dermis ( Fig. 1B ). These pathologic findings were consistent with first stage IP. Pathologic examination of skin biopsy from the vesicles located on the scalp of the twins revealed multinucleated giant cells and balloon cells around the keratinocytes (Fig. 2B). Ophtholmologic examination of the twin B demonstrated retinopathy which consisted of venous engorgement and soft exudates on the retina. Results of bacterial culture from the vesicles located on the scalp, trunk and legs were negative. Tzanck smear from the vesicles located on the trunk, limbs and scalp showed different results. The results of scrapings taken from the trunk and limbs were negative; but from the scalp, we found multinucleated giant cells. Viral culture and monoclonal antibody immunofluorescene proved that there was HSV, type II infection. Viral cultures of the eyes of the twin A were positive for herpes virus. Viral cultures of nasopharynx and cerebrospinal fluid were negative. Except the ocular problems, the twins did not have any other systemic complications such as seizures, encephalitis or skeletal anomalies. Chromosomal studies of the twins showed the normal karyotype 46, XX and no translocation or other chromosome aberration. Our diagnosis was first stage IP and concurrent neonatal HSV infection. To prevent disseminated HSV infection, they received intravenous and topical acyclovir treatment. When the condition of the female twins became stable, they were discharged and followed up regularly at our hospital. 295 DISCUSSION The diagnosis of an inherited cutaneous condition does not exclude the possibility of a coexistence infection and, given the similar clinical presentation of neonatal vesicular eruptions, accurate diagnosis may require skin biopsy and culture. There have been two published articles that reported incontinentia pigmenti and concurrent neonatal herpes simplex virus infection.5, 6 Incontinentia pigmenti ( IP ) is a rare Xlinked dominantly genetic disease with characteristic skin manifestations. This disorder has four stages.7 The first (erythema and vesicular) stage is either present at birth or starts shortly thereafter. It is characterized by linear vesicular eruptions primarily on the extremities and occasionally on the trunk. IP is associated with several abnormalies in the systems such as central nervous system, eyes and teeth.7 Ocular abnormalities occur in about 35 % of patients and consist of proliferative vitreoretinopathy, retinal detachment, strabismus, cataract, microphthalmia, and optic nerve atrophy.8 Although our chromosomal studies of the twins showed the normal karyotype and no translocation or other chromosome aberration, we did not exclude the possibility of genetic disorder. Several articles about genetic studies discovered an IP locus at Xq28 which was mapped on the basis of findings from cytogenetic and linkage analysis. Newest genetic studies have demonstrated that mutations in a single gene result in the IP phenotype.9-13 While IP is a rare disease, neonatal herpes simplex virus ( HSV ) infection may affect 1 in 2000 deliveries. HSV infection of the newborns is usually related to maternal asymptomatic first episode infection in the birth canal during late pregnancy. 3 Any area of the skin may be involved, but the grouped vesicles are most commonly present on the scalp or buttock. Monitoring electrodes may produce sufficient skin trauma through which the virus can invade. On rare instance, neonatal HSV lesions may display a linear distribution. Vesicles rarely present at birth. The incubation period of Dermatol Sinica, September 2003 ّ̃ᗕࡪࡩ۞Ғ৵ε༰াЪ׀າϠಏ৷ neonatal herpes is 2 to 21 days and the mean age of onset is 6 days. Eighty percent neonatal infections are HSV-2.3, 4, 14 Neonatal HSV infections are frequently limited to skin, eyes and mucous membranes, but disseminated infection which invades the central nervous system with severe neurodevelopmental sequelae or death can occur.4 The ocular manifestations of herpes infection consist of anterior uveitis and keratitis.15, 16 The majority of these infected newborns present with nonspecific symptoms and signs, such as irritability, lethargy, fever, or failure to feed. Until the disease is far advanced, the diagnosis of neonatal herpes is often ignored. So we should keep in mind that concurrent HSV infection would be in the differential diagnosis of the neonatal blistering diseases because it may complicate the management of infants with IP.5, 6 There have been two published articles about newborns with IP and concurrent neonatal HSV infection.5, 6 In our cases, maternal first episode genital herpes in the late pregnancy led to neonatal HSV infection during labor and delivery. Because maternal HSV seroconversion had not been completed by the time of labor, the newborns did not have the protective antibody against HSV invasion. As mentioned to the ocular complications, the cause of retinopathy was a manifestation of IP - associated anomalies. Although viral cultures of the eyes were positive for herpes virus, no residual neurologic or ocular complications have been detected after preventive intravenous and topical acyclovir treatment. Because the course and management of IP and HSV infection is quite different, we suggest that both of the diseases need to be considered in the differential diagnosis of neonatal blistering disorders. REFERENCES 1. Gorski JL, Burright EN: The molecular genetics of incontinentia pigmenti. Semin Dermatol 2: 255-265, 1993. 2. Sybert VP. Principles of genetics in the molecular era: a primer for dermatologists. Arch Dermatol 129: 1409-1416, 1993. 3. Brown ZA, Benedetti J, Ashley R, et al.: Dermatol Sinica, September 2003 ৃঽ߲ຏߖ Neonatal herpes simplex virus infection in relation to asymptomatic maternal infection at the time of labor. N Engl J Med 324: 1247-1252, 1991. 4. Whitley R, Arvin A, Prober C, et al.: Predictors of morbidity and mortality in neonates with herpes simplex virus infections. N Engl J Med 324: 450-454, 1991. 5. Stitt WZ, Scott GA, Caserta M, et al.: Coexistence of incontinentia pigmenti and neonatal herpes simplex virus infection. Pediatr Dermatol 15: 112-115, 1998. 6. Fromer ES, Lynch PJ: Neonatal herpes simplex and incontinentia pigmenti. Pediatr Dermatol 18: 86-87, 2001. 7. Landy SJ, Donnai D: Incontinentia pigmenti (Bloch-Sulzberger syndrome). J Med Genet 30: 53-59, 1993. 8. Nguyen JK, Brady-Mccreery KM: Laser photocoagulation in preproliferative retinopathy of incontinentia pigmenti. JAAPOS: Am Asso Pediatr Ophthalmol Strabismus. 5: 258-259, 2001. 9. Sefiani A, Abel L, Heuertz S, et al.: The gene for incontinentia pigmenti is assigned to Xq28. Genomics 4: 427-429, 1989. 10. Smahi A, Hyden-Granskog C, Peterlin B, et al.: The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28. Hum Mol Genet 3: 273-278, 1994. 11. Jin DY, Jeang KT: Isolation of full-length cDNA and chromosomal localization of human NF-kappaB modulator NEMO to Xq28. J Biomed Sci 6: 115-120, 1999. 12. Smahi A, Courtois G, Vabres P, et al.: Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. Nature 405: 466-472, 2000. 13. Berlin AL, Paller AS, Chan LS: Incontinentia pigmenti: a review and update on the molecular basis of pathophysiology. J Am Acad Dermatol 47: 169-187, 2002. 14. Kulhanjian JA, Soroush V, Au DS, et al.: Identification of women at unsuspected risk 296 ࣫ܫඕ of primary infection with herpes simplex virus type 2 during pregnancy. N Engl J Med 326: 916-920, 1992. 15. Siverio Junior CD, Imai Y, Cunningham ET Jr: Diagnosis and management of herpetic anterior uveitis. Int Ophthalmol Clin 42: 43- 297 48, 2002. 16. Tabery HM: Epithelial changes in early primary herpes simplex virus keratitis. Photomicrographic observations in a case of human infection. Acta Ophthalmol Scand 78: 706-709, 2000. Dermatol Sinica, September 2003