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| LETTER TO EDITOR |
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| Year : 2017 | Volume
: 9
| Issue : 3 | Page : 138-139 |
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Keratosis follicularis spinulosa decalvans with associated mental retardation: response to isotretinoin
Sarita Sanke, Vibhu Mendiratta, Archana Singh, Ram Chander
Department of Dermatology and Sexually Transmitted Diseases, Lady Hardinge Medical College and Suchita Kriplani Hospital, Shaheed Bhagat Singh Marg, New Delhi, India
| Date of Web Publication | 21-Aug-2017 |
Correspondence Address:
Sarita Sanke
Room No. 220, HSB Hostel, Lady Hardinge Medical College, New Delhi - 110 001
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijt.ijt_25_17
How to cite this article:
Sanke S, Mendiratta V, Singh A, Chander R. Keratosis follicularis spinulosa decalvans with associated mental retardation: response to isotretinoin. Int J Trichol 2017;9:138-9 |
How to cite this URL:
Sanke S, Mendiratta V, Singh A, Chander R. Keratosis follicularis spinulosa decalvans with associated mental retardation: response to isotretinoin. Int J Trichol [serial online] 2017 [cited 2023 Mar 29];9:138-9. Available from: https://www.ijtrichology.com/text.asp?2017/9/3/138/213341 |
Sir,
Keratosis follicularis spinulosa decalvans (KFSD), a rare disorder that was originally described by Siemens, often starts at infancy or early childhood with an X-linked mode of inheritance. Males are predominantly affected. It is characterized by photophobia, corneal dystrophy, widespread follicular hyperkeratosis, scarring alopecia of the scalp, eyebrows, and eyelashes. We report an 18-year-old boy, born of nonconsanguineous marriage, who presented with rough, keratotic papules over the scalp, neck, upper, and lower limbs, along with alopecia since birth. There was sparse growth of hairs over these papules which eventually shed off. There was no history of atopy, ichthyosis, photophobia, hypo or hyperhidrosis, skeletal abnormality, and eye or ear complaints. A family history was not contributory. Physical examination showed multiple follicular dark brown to black, monomorphic, keratotic papules over the scalp, neck, and other areas of the body (upper/lower limb and trunk) along with scarring alopecia over the scalp [Figure 1]. Pubic hairs were normal but hairs over axilla, eyebrows, eyelashes, and beard were sparse. The oral cavity, nails, palms, and soles were found to be normal. Rest of the systemic evaluation revealed no abnormal findings. Hair shaft microscopic examination revealed no abnormality. Neuropsychiatric evaluation revealed a borderline mental retardation (Intelligence quotient-60). Histopathology from a keratotic papule over the scalp showed follicular plugging, basket weave orthokeratosis, mild perivascular inflammatory infiltrate along with perifollicular fibrosis and a small vertical scar [Figure 2]. Magnetic resonance imaging brain did not reveal any abnormal finding. With all the above finding, a diagnosis of KFSD in association with mental retardation was made. Our patient was started on oral isotretinoin (0.5 mg/kg). Following 1 month of therapy, there was marked flattening of the keratotic papules, and significant hair growth was seen by the 3rd month [Figure 3]. He was followed up for the next 6 months. | Figure 2: Follicular plugging, perifollicular fibrosis, and vertical scar (H and E, ×40)
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The locus of mutation of KFSD has been localized to Xp22.[1] The candidate gene suggested is the membrane-bound transcription factor protease site 2 gene which is required for cleavage of sterol regulatory element-binding proteins (SREBPs). Altered SREBP cleavage impairs cholesterol and lipid homeostasis in the skin causing defective epidermal differentiation.[2]
The skin manifestations usually appear during the 1st weeks or months of life and are characterized by follicular hyperkeratosis of the skin, especially in the region of the face, associated with scarring alopecia and absence of the follicles of the hair, eyelashes, and eyebrows. Eye symptoms can be associated, the most typical of which are photophobia, keratitis, conjunctivitis, congenital glaucoma, lenticular cataract, and corneal dystrophy.[3] Some patient have associated features including palm plantar keratoderma and the unusual sign of long cuticles.[4] Our patient had associated mental retardation with a subnormal IQ. This is a rare finding associated with KFSD, with only 1 case report previously reported.[5] Other less commonly reported features are atopy, deafness, mental retardation, acne keloidalis nuchae, tufted hair folliculitis, aminoaciduria, and woolly hair.[6],[7],[8],[9]
Treatment of KFSD is usually unsatisfactory. Topical treatment comprises mainly of keratolytics and emollients. Systemic retinoids such as isotretinoin and etretinate are beneficial in the early stages of the disease as they downregulate follicular hyperkeratosis and inflammation.[10] The condition is found to recur after stopping the treatment; however, our patient showed no recurrence in the 6 months of follow-up. Other treatment options such as tetracyclines, sulfonamides (dapsone), macrolides, penicillins, and rifampin have been found to be ineffective.[11] Topical and intralesional corticosteroids were tried but cause only transient improvement. Laser assisted hair removal with the long-pulse non-Q-switched ruby laser has been found to be useful in progressive or recalcitrant KFSD.[12]
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
 References | |  |
| 1. | Porteous ME, Strain L, Logie LJ, Herd RM, Benton EC. Keratosis follicularis spinulosa decalvans: Confirmation of linkage to Xp22.13-p22.2. J Med Genet 1998;35:336-7.  |
| 2. | Aten E, Brasz LC, Bornholdt D, Hooijkaas IB, Porteous ME, Sybert VP, et al. Keratosis follicularis spinulosa decalvans is caused by mutations in MBTPS2. Hum Mutat 2010;31:1125-33. |
| 3. | Rand R, Baden HP. Keratosis follicularis spinulosa decalvans. Report of two cases and literature review. Arch Dermatol 1983;119:22-6. |
| 4. | van Osch LD, Oranje AP, Keukens FM, van Voorst Vader PC, Veldman E. Keratosis follicularis spinulosa decalvans: A family study of seven male cases and six female carriers. J Med Genet 1992;29:36-40. |
| 5. | Masood Q, Manzoor S, Hassan I, Majid I. Psychomotor retardation – An unusual association of keratosis follicularis spinulosa decalvans. Indian J Dermatol Venereol Leprol 2000;66:320-1. [ PUBMED] [Full text] |
| 6. | Britton H, Lustig J, Thompson BJ, Meyer S, Esterly NB. Keratosis follicularis spinulosa decalvans. An infant with failure to thrive, deafness, and recurrent infections. Arch Dermatol 1978;114:761-4. |
| 7. | Grosshans E, Heid E, Stoll C. Keratosis follicularis spinulosa decalvans and amino-aciduria. Ann Dermatol Venereol 1978;105:433-8. |
| 8. | Lacarrubba F, Dall'Oglio F, Rossi A, Schwartz RA, Micali G. Familial keratosis follicularis spinulosa decalvans associated with woolly hair. Int J Dermatol 2007;46:840-3. |
| 9. | Janjua SA, Iftikhar N, Pastar Z, Hosler GA. Keratosis follicularis spinulosa decalvans associated with acne keloidalis nuchae and tufted hair folliculitis. Am J Clin Dermatol 2008;9:137-40. |
| 10. | Richard G, Harth W. Keratosis follicularis spinulosa decalvans. Therapy with isotretinoin and etretinate in the inflammatory stage. Hautarzt 1993;44:529-34. |
| 11. | Baden HP, Byers HR. Clinical findings, cutaneous pathology, and response to therapy in 21 patients with keratosis pilaris atrophicans. Arch Dermatol 1994;130:469-75. |
| 12. | Chui CT, Berger TG, Price VH, Zachary CB. Recalcitrant scarring follicular disorders treated by laser-assisted hair removal: A preliminary report. Dermatol Surg 1999;25:34-7. |
[Figure 1], [Figure 2], [Figure 3]
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