CASE REPORT
Year : 2016 | Volume
: 8 | Issue : 3 | Page : 141--143
Mayer-Rokitansky-Küster-Hauser syndrome with alopecia: A rare case report with review of literature
Sanjiv V Choudhary, Uday V Choudhari
Department of Dermatology Venereology and Leprosy, Jawaharlal Nehru Medical College, Sawangi (Meghe), Wardha, Maharashtra, India
Correspondence Address:
Sanjiv V Choudhary
28, Modern Nagpur Society, Chatrapati Nagar, Nagpur, Maharashtra
India
Abstract
A 17-year-old girl presented with alopecia involving lateral margins of the scalp with primary amenorrhea. There was no history of parental consanguinity, and no other siblings were having similar complaints. Her secondary sexual characters were well developed with hypoplastic vagina. Histopathological findings from scalp biopsy showed features of alopecia areata. Ultrasonography of abdomen and pelvis revealed the absence of uterus and the right kidney. Follicle-stimulating hormone, luteinizing hormone, estradiol, testosterone, and thyroid function test was within normal limits. The patient had normal 46, XX Karyotype. Till date, only four case reports of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome with alopecia has been reported. We are reporting the first case of MRKH syndrome with alopecia with normal gonadal function in world«SQ»s literature.
How to cite this article:
Choudhary SV, Choudhari UV. Mayer-Rokitansky-Küster-Hauser syndrome with alopecia: A rare case report with review of literature.Int J Trichol 2016;8:141-143
|
How to cite this URL:
Choudhary SV, Choudhari UV. Mayer-Rokitansky-Küster-Hauser syndrome with alopecia: A rare case report with review of literature. Int J Trichol [serial online] 2016 [cited 2023 Mar 29 ];8:141-143
Available from: https://www.ijtrichology.com/text.asp?2016/8/3/141/189012 |
Full Text
Introduction
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome or Mullerian duct agenesis is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. Till date, there are only four case reports of MRKH syndrome with alopecia. [1],[2],[3],[4] The presence of alopecia with MRKH syndrome is a mere coincidence or an associated finding is a subject of research and may require further evidence.
Case Report
A 17-year-old girl presented with hair loss from the scalp for 1 year. She also had a history of primary amenorrhea. The loss of hair begins at the occipital area of the scalp, and it progressed along the lateral margins of the scalp in a band like fashion clinically suggestive of ophiasis type of alopecia areata. The follicular openings were well preserved with normal skin texture [Figure 1]a. Detailed gynecological examination revealed normal secondary sexual characters with well-developed external genitalia and hypoplastic vagina [Figure 1]b. The histopathology of the scalp revealed lymphocytic infiltration around the lower third of the hair follicle, a finding suggestive of alopecia areata. To rule out the cause of amenorrhea, ultrasonograhy of abdomen and pelvis was done which revealed the absence of uterus and right kidney with normal ovaries [Figure 2]a and b. Hormone levels (follicle-stimulating hormone, luteinizing hormone, estradiol, testosterone, and thyroid function test) were within normal limits. The karyotyping showed 46 XX.{Figure 1}{Figure 2}
Discussion
The detailed review of four case reports of MRKH syndrome with alopecia in world's literature has been given in [Table 1]. First, three reports were from the same geographical region of Middle East (Jordan, Lebanon, and Turkey, respectively). [1],[2],[3] Megerbane et al. [2] and Tatar et al. [3] hypothesized that the founder mutation in Middle East population might be responsible for the condition to be restricted to that geographical region.However, the fourth case report from South Asia (Pakistan) questioned the hypothesis of founder mutation leading to MRKH syndrome restricted to that geographical region. [4] We are reporting the fifth case report which is the second case report from South Asia and first among Indian population. Our case report is another evidence to suggest that MRKH syndrome with alopecia is not restricted to Middle East population.{Table 1}
In all previously reported four case reports, there was a history of parental consanguinity and siblings were also affected with MRKH syndrome and alopecia. In our case, there was no history of parental consanguinity and siblings were normal. There are many case reports and syndromes of hypogonadism with alopecia. [5],[6],[7] In all the previous case reports of MRKH syndrome with alopecia, hypergonadotropic hypogonadism was noted. This case is the first report of MRKH syndrome with alopecia with normal gonadal function. MRKH syndrome may have associated abnormalities such as renal agenesis, skeletal abnormalities, hearing loss, or cardiac defects. [8],[9] In our case, the right renal agenesis was the associated finding of MRKH syndrome with alopecia which is not observed in all the previous four case reports under review.
In a female patient of alopecia areata, history of primary amenorrhea may be important to rule out the rare association with MRKH syndrome. This syndrome is caused by embryologic growth failure of the Mullerian duct with resultant agenesis or underdevelopment of the vagina, uterus or the both. All the reported cases of MRKH with alopecia including our case had alopecia areata which is an autoimmune disease. There seems to be no direct correlation between these entities as one is due to a genetic defect, and other is an autoimmune disease. Hence, the presence of alopecia in the case of MRKH syndrome is a mere coincidence, or an associated finding of the syndrome is a matter of further study.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References
| 1 | Al-Awadi SA, Farag TI, Teebi AS, Naguib K, el-Khalifa MY, Kelani Y, et al. Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females. Am J Med Genet 1985;22:619-22. |
| 2 | Mégarbané A, Gannagé-Yared MH, Khalifé AA, Fabre M. Primary hypergonadotropic hypogonadism, partial alopecia, and Müllerian hypoplasia: Report of a second family with additional findings. Am J Med Genet A 2003;119A: 214-7. |
| 3 | Tatar A, Ocak Z, Tatar A, Yesilyurt A, Borekci B, Oztas S. Primary hypogonadism, partial alopecia, and Mullerian hypoplasia: Report of a third family and review. Am J Med Genet A 2009;149A: 501-4. |
| 4 | Zaman SM, Nisar M. Primary hypergonadotrophic hypogonadism, alopecia totalis, and müllerian hypoplasia: A clinical study. J Pak Med Assoc 2009;59:571-3. |
| 5 | Crandall BF, Samec L, Sparkes RS, Wright SW. A familial syndrome of deafness, alopecia, and hypogonadism. J Pediatr 1973;82:461-5. |
| 6 | Johnson VP, McMillin JM, Aceto T Jr., Bruins G. A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism. Am J Med Genet 1983;15:497-506. |
| 7 | Slti IS, Salem Z. Familial hypogonadotropic hypogonadism with alopecia. Can Med Assoc J 1979;121:428-30, 433-4. |
| 8 | Shah VN, Ganatra PJ, Parikh R, Kamdar P, Baxi S, Shah N. Coexistence of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome in 46, XX female: A case report and review of literature. Indian J Endocrinol Metab 2013;17 Suppl 1:S274-7. |
| 9 | Patnaik SS, Brazile B, Dandolu V, Ryan PL, Liao J. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: A historical perspective. Gene 2015;555:33-40. |
|
