Darier's disease mimicking condyloma accuminata, unusual presentation: a case report.
CASE REPORT: A 35 year old female born to non-consanguineous marriage, presented with skin lesions of 15 years duration, consisting of multiple brown black, warty, greasy, follicular and non-follicular papules, some of which also showed keratin plugs, mainly over the seborrhoeic areas, few papules were also present over the dorsa of fingers, hands, feet and both shins. Red and white bands and V shaped nicking at the free margins were noted on the finger nails. Hyperkeratotic verrucous (Warty) growth present over the external genitalia and preianal area, few areas showing erosions. [Fig. 1 & Fig. 2]
Routine investigations were within normal limits. VDRL, HIV1 & 2 and HbsAg were negative. Punch biopsy from the lower back and excision biopsy from external genitalia were showed hyperkeratosis, suprabasal lacunae, corps-ronds and grains and hyperkeratotic invagination filled with keratinous material and acantholytic cells suggestive of Darier's disease. [Fig. 3]
DISCUSSION: The disease was first reported independently by Darier and White in 1889. Darier's disease (DD) is a rare congenital acantholytic disorder transmitted as an autosomal dominant trait. It may also occur as mutation. Both sexes are affected with equal frequency. It usually begins in childhood but can manifest at any time. (3)
Mutation in the gene ATP2A2 cause Darier's disease. ATP2A2 located on 12q23-24, encodes the endoplasmic reticulum Ca 2+ ATP, which is a calcium pump. This pump maintains low cytoplasmic Ca2+ve level by actively transporting Ca ions from the cytosol in to the lumen of the endoplasmic reticulum. (4)
Electron microscopy reveals loss of desmosomes, breakdown of desmosome-keratin intermediate filament attachment, and perinuclear aggregates of keratin intermediate filaments. (5)
The lesion may first appear as skin colored or yellow brown papules with a greasy, warty texture. The lesion are especially common in seborrhoeic areas such as the forehead, scalp, margin of the scalp, nasolabial folds, ears, chest and back. In less than 10% of patients, flexural disease predominates, with large, warty, vegetative papules in the axillae, groins or perineum. Frequently associated with pruritus. Heat, sweat, humidity, sunlight, UVB exposure, lithium, oral corticosteroids and mechanical trauma have been reported to exacerbate this condition. (6)
Involvement of hands include punctate keratosis, palmar pits and haemorrhagic macules, acrokeratosis verruciformis like lesions are present in half the patients. Nail changes like white and red longitudinal bands, longitudinal ridges, V shaped nick and subungual hyperkeratosis are frequently found. (7) Mucosal lesions appear as white papules with a central depression (cobblestone) lesions commonly seen in the mouth, but can also occurs in genital mucosa. (8)
The histopathological finding, irrespective of clinical presentation, characterized by focal changes of acantholysis and presence of dyskeratotic cells resembling Corps ronds and grains associated with suprabasal clefts around the preserved villi, hyperkeratosis and parakeratosis. These findings are classical of Darier's disease, but are also found in Hailey Hailey disease, Grover's disease and warty dyskeratoma. (9)
In 1984, Chorzelski et al reported a 23-year old female with multiple asymptomatic dome-shaped papules on the labia majora. Clinically, this was different from Hailey-Hailey disease in that papules were persistent for more than six years and there were no vesicles, fissuring and erosions. Histology showed hyperkeratosis, parakeratosis with some areas showing intraepidermal vesiculation and acantholysis similar to Hailey-Hailey disease, while other areas were more like Darier's disease showing dyskeratotic cells throughout the epidermis, including Corps ronds and grains. Skin and serum immunofluorescence were negative. The author regarded this as a new entity and named the disease as Papular acantholytic dyskeratosis (PAD).
PAD is an uncommon disorder of the genitalia, usually asymptomatic but sometimes may be pruritic. It is more commonly reported in females, with lesions occurring on the vulva and perianal area, but there has also been a report of a male patient with lesions over the penile shaft. (10) Clinically, PAD must be differentiated from genital papules of infectious origin, Hailey-Hailey disease, localized Darier's disease of genital area and various pre-malignant and malignant conditions. (9)
In our case female patient presented with condyloma accuminata like growth over external genitalia and perianal area, which is rare clinical morphology of Darier's disease and confirmed by histological findings. It is clinically differentiated by PAD and histologically by warty dyskeratoma. We are reporting this case for its morphological rarity.
(1.) Lever WF and Schaumburg-Lever G: Congenital diseases (Genodermatoses), in: Histopathology of skin, 6th Ed, JB Lippincott Company, Philadelphia, 1983; p 70.
(2.) Griffiths WAD, Leigh IM, Markss R.Disorders of keratinizationn. In: Textbook of Dermatology (champion RH, Burton JL, Ebling FJG, eds), 5th edn. Oxford: Blackwell Scientific, 1992; 1362-5.
(3.) Burge SM, Wilkinson JD, Darier-White disease: a review of the clinical features in 163 patients. J Am Acad Dermatology 1992; 168-171.
(4.) Sakuntabhai, Burge S, Monk S et al. Spectrum of novel ATP2A2 mutation causes segmental Darier's disease. Hum Mol Genet 1999; 8: 1611-9.
(5.) Garrod D, Merritt A, Nie Z. Desmosomal cadherins. Curr Opin Cell Biol 2002; 14: 537.
(6.) Getzler MA, flint A. Keratosis follicularis. A study of one family. Arch Dermatol 1973; 132: 545-9.
(7.) Zaias N, Ackerman AB. The nail in Darier-White disease. Arch Dermatol 1973; 107: 193-9.
(8.) Byrge S. Darier's disease--the clinical features and pathogenesis. Dermatology 1999; 199: 365-8.
(9.) Roh MR, Choi YJ, Lee KG. Papular acantholytic dyskeratosis of the vulva. J Dermatol 2009; 36: 427-9.
(10.) Chorzelski TP, Kudejko J, Jablonska S. Is papular acantholytic dyskeratosis of the vulva a new entity? Am J Dermpatopathol 1984; 6: 557-9.
[FIGURE 1 OMITTED]
[FIGURE 2 OMITTED]
[FIGURE 3 OMITTED]
Raghu M. T , Parvathi C. N , Kavya Shree K. L , Yogendra M , Girish N 
[1.] Raghu M. T.
[2.] Parvathi C. N.
[3.] Kavya Shree K. L.
[4.] Yogendra M.
[5.] Girish N.
PARTICULARS OF CONTRIBUTORS:
[1.] Assistant Professor, Department of Dermatology, BMCH & RC, Chitradurga.
[2.] Professor and HOD, Department of Dermatology, BMCH & RC, Chitradurga.
[3.] Senior Resident, Department of Dermatology, BMCH & RC, Chitradurga.
[4.] Professor, Department of Dermatology, BMCH & RC, Chitradurga.
[5.] Assistant Professor, Department of Dermatology, BMCH & RC, Chitradurga.
NAME ADDRESS EMAIL ID OF THE CORRESPONDING AUTHOR:
Dr. Raghu M. T, Assistant Professor, Department of Dermatology, BMCH & RC, Chitradurga.
Date of Submission: 08/12/2014.
Date of Peer Review: 09/12/2014.
Date of Acceptance: 15/12/2014.
Date of Publishing: 22/12/2014.
|Printer friendly Cite/link Email Feedback|
|Title Annotation:||CASE REPORT|
|Author:||Raghu, M.T.; Parvathi, C.N.; Kavya, Shree K.L.; Yogendra, M.; Girish, N.|
|Publication:||Journal of Evolution of Medical and Dental Sciences|
|Date:||Dec 22, 2014|
|Previous Article:||Lithoptysis associated with chronic pulmonary tuberculosis.|
|Next Article:||To find out change in knowledge and attitude towards HIV/AIDS of 1st year and IVth year MBBS students.|