|Year : 2016 | Volume
| Issue : 4 | Page : 275-277
Dyskeratosis congenita presenting with dysphagia
Kalpana Gupta, Swati Tripathi, Nidheesh Agarwal, Anurag Bareth
Department of Dermatology, Venereology and Leprosy, Geetanjali Medical College and Hospital, Udaipur, Rajasthan, India
|Date of Web Publication||5-Jul-2016|
Flat No. 001, Fateh Apartment, New Fatehpura, Udaipur - 313 001, Rajasthan
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Dyskeratosiscongenita (DKC) is a genetically heterogeneous disease of defective telomere maintenance that may demonstrate different patterns of inheritance. It is characterized by thetriad of dystrophy of the nails, leukokeratosis of the oral mucosa, and extensive net-like pigmentation of the skin. We report a case ofDKC who presented with a chief complaint of dysphagia.
Keywords: Dyskeratosis congenita, dysphagia, leukoplakia, nail dystrophy, reticulate hyperpigmentation
|How to cite this article:|
Gupta K, Tripathi S, Agarwal N, Bareth A. Dyskeratosis congenita presenting with dysphagia. Indian Dermatol Online J 2016;7:275-7
|How to cite this URL:|
Gupta K, Tripathi S, Agarwal N, Bareth A. Dyskeratosis congenita presenting with dysphagia. Indian Dermatol Online J [serial online] 2016 [cited 2019 Dec 10];7:275-7. Available from: http://www.idoj.in/text.asp?2016/7/4/275/185461
| Introduction|| |
DyskeratosisCongenita (DKC) or the Zinsser–Cole–Engman syndrome is a multisystem genetic disease characterized by a triad of pigmentation and atrophy of skin, nail dystrophy, and leukoplakia. Multisystem involvement (dental, gastrointestinal, genitourinary, neurological, ophthalmic, pulmonary, and skeletal) isknown. We report a case of recurrent dysphagia under care of gastroenterologist, which was referred to us for cutaneous, oral, and nail lesions. He was diagnosed to have DKC; his dysphagia was part of systemic involvement of DKC.
| Case Report|| |
An 18-year-old boy, born of a nonconsanguineous marriage, presented to the hospital emergency with a three-day history of dysphagia. The patient gave a history of two similar episodes of dysphagia that were relievedon treatment. He was under the care of a gastroenterologist who performed an endoscopy and a barium swallow that revealed a very tight stricture at the upper end of esophagus [Figure 1]. It was diagnosed asacongenital web and dilated after passing a guide wire. He was referred to dermatology departmentfor pigmentation of skin and nail dystrophy. A detailed history revealed that the patient developed splitting and dystrophy of his fingernails and toenails at 5 years of age. This was followed by pigmentation of the skin within a year. Pigmentation first appeared on the neck and lower limbs, followed by the extensive involvement of the entire body with sparing of the face. Around this time he started developing oral ulcers that were recurrent despite treatment. He gave no history of eye complaints, loss of hair, dental caries, or difficulty in keeping up with studies. Except dysphagia, patient gave no history of systemic symptoms. The patient's maternal uncle had a history of similar type of skin pigmentation and nail dystrophy, and died of unknown causes at 55 years of age.
A thorough examination of the patient revealed generalized fine, lacy, reticulated, greyish-brown pattern of hyperpigmentation with areas of epidermal atrophy (poikiloderma), sparing the face [Figure 2]a and [Figure 2]b. Examination of the genitals revealed no signs of testicular atrophy. Splitting of nails with pterygium formation and dystrophy was present, more over the fingers than the toes [Figure 2]c. Examination of the oral mucosa revealed the presence of a whitish, well-defined leukoplakic plaque on the dorsal surface of the tongue, interrupted by lingual ulcers [Figure 2]d. Buccal and labial mucosa were spared. There were no significant systemic findings. Routine investigations along with skin biopsy were done. Histopathological examination of skin sample revealed melanophages in the upper dermis and vacuolization of basal cells. Routine investigations of the patient were normal. Bone marrow biopsy and lingual biopsy were refused by the patient. The classic clinical findings, family history and consistent histopathology enabled us to make a diagnosis of DKC.
|Figure 2: Patient having classical features of dyskeratosis congenita which include (a and b) reticulate pigmentation (c) nail dystrophy (d) oral leukoplakia with ulceration|
Click here to view
| Discussion|| |
DKC (Zinsser–Cole–Engman syndrome) is a rare disorder of telomere biology, estimated to affect 1 in 1 million people and transmitted as an X-linked recessive (which is the most common), autosomal dominant or autosomal recessivetrait. It is characterized by the classic triad of dystrophic nails, lacy reticular pigmentation of the upper part of chest and/or neck, and oral leukoplakia. Nail changes are the first to appear and lead to splitting, dystrophy, and shedding of nails. Reticulate pigmentation and atrophy of epidermis (poikiloderma) also manifests simultaneously, or within 2–3 years. Mucous membrane lesions are common such as blisters and erosions of the lingual and buccal mucous membrane, which are succeeded by irregular patches of leukoplakia. Other mucous membranes such as conjuctival, anorectal, esophageal (or throughout the gastrointestinal mucosa) and urethral mucosa may get involved causing leukoplakia and/or stenosis. Other reported dermatological manifestations include palmoplantar thickening and hyperhidrosis, premature canities, and cicatricialalopecia. The teeth tend to be defective and irregularly implanted, and periodontal disease and early caries are usual. General physical and mental development is sometimes delayed, and osteoporosis may occur. Immunodeficiency, intrauterine growth retardation, microcephaly, cerebellar hypoplasia, and intracranial calcification have also been reported. Prognosis is usually poor, as either blood dyscrasias (bone marrow failure, pancytopenia) or malignancies (carcinoma of mouth, Hodgkin's disease and pancreatic adenocarcinoma) may prove fatal.
Our patient presented with chief complaints of recurrent dysphagia, which had been treated in the past with endoscopic dilatation. This was the patient's third episode. On examination, was found to have the classical triad of DKC which enabled us to make thediagnosis. Although dysphagia has been reported in DKC,,,, it is not a very common finding and it is unusual for patients to present with it as the chief complaint. Other positive findings included family history, hyperhidrosis of palms and soles, and premature greying of hair.
This case is being reported because it is a rare disease that presented to us in an uncommon manner. Dermatologists should be aware of the possibility of esophageal involvement, and history regarding dysphagia should be taken in patients of DKC. Also, the diagnosis of DKC could be made because the physician sought the help for interpreting the dermatologic findings. The authors want to stress the importance of multidisciplinary care in healthcare institutions. More often than not, it helps in establishment of correct diagnosis and better healthcare delivery through prognostication, genetic counseling, and appropriate management.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Irvine AD, Mellerio JE. Genetics and genodermatoses. In: Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook's Textbook of Dermatology. 8th
ed. West sussex: Wiley-Blackwell; 2010.p. 15.78-9.
Savage SA, Alter BP. The role of telomere biology in bone marrow failure and other disorders. Mech Ageing Dev2008;129:35-47.
Milgrom H, Stoll HJ Jr, Crissey JT. Dyskeratosiscongenita. A case with new features. Arch Dermatol1964;89:345-9.
Knight S, Vulliamy T, Copplestone A, Gluckman E, Mason P, Dokal I. Dyskeratosiscongenita (DC) registry: Identification of new features of DC. Br J Haematol1998;103:990-6.
Berezin S, Schwarz SM, Slim MS, Beneck D, Brudnicki AR, Medow MS. Gastrointestinal problems in a child with dyskeratosiscongenita. Am J Gastroenterol 1996;91:1271-2.
Ogden GR, Connor E, Chisholm DM. Dyskeratosiscongenita: Report of a case and review of the literature. Oral Surg Oral Med Oral Pathol 1988;65:586-91.
Lorette G, Guérois M, Arbeille-Brassart B, De Russe MY, Binet C Boulard P, et al
. Dyskeratosiscongenita Zinsser-Cole-Engman form. Report of two affected brothers. Ann DermatolVenereol 1980;107:799-805.
Chong LA, Ariffin H. A rare X-linked inherited mucocutaneous syndrome in two siblings. Med J Malaysia 2009;64:327-9.
[Figure 1], [Figure 2]