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CASE REPORT
  
Year : 1994  |  Volume : 60  |  Issue : 3  |  Page : 168-169

Perforating granuloma annulare

RR Mittal, AK Chopra, RLS Walia, Rita Dutt, S Gill 
 

Correspondence Address:
R R Mittal


Abstract

Perforating Granuloma annulare (GA) of palmar surfaces of both index fingers was observed in a 41 years female. Duration was 1½ years and papules were asymptomatic, yellow, firm, discrete, with central pits. FBS was 81 mg/dl. Histopathology revealed transepidermal elimination of altered collagen, foci of degenerated collagen surrounded by groups of mononuclears admixed with occassional eosinophil and giant cell in irregular palisade arrangement.



How to cite this article:
Mittal R R, Chopra A K, Walia R, Dutt R, Gill S. Perforating granuloma annulare.Indian J Dermatol Venereol Leprol 1994;60:168-169


How to cite this URL:
Mittal R R, Chopra A K, Walia R, Dutt R, Gill S. Perforating granuloma annulare. Indian J Dermatol Venereol Leprol [serial online] 1994 [cited 2020 Feb 23 ];60:168-169
Available from: http://www.ijdvl.com/text.asp?1994/60/3/168/4030


Full Text

 Introduction



GA can present in localised form, generalised or widely diseminated form, as subcutaneous nodules and perforating papules. [1] Perforating GA may heal with hypo or hyperpigmented scars; [2] In perforating GA umbilicated papules over the hands develop a yellowish centre due to transepidermal elimination of altered dermal collagen. [3] Generalised perforating GA has been reported. [4] Histopathologically perforating GA show transepidermal elimination of degenerated collagen, small to large foci of collagen degeneration with mucin at places, surrounded by histiocytes in palisade arrangement, vasculitis, lymphoid cells, occasional giant cells and fibroblasts. [5]

 Case Report



A 41-years-old female had multiple, asymptomatic, progressive, firm, well defined, flat papules and plaques on palmar surface of both index fingers since 1 [1]/2 years [Figure 1]. Old papules resolved spontaneously after 3-4 months while new ones appeared. Papules and plaques had central depression where skin surface was rough, although retaining intact dermatoglyphic pattern of ridges alternating with depression. FBS was 81 mg/dl. Histopathology revealed hyperkeratosis and multiple channels in epidermis through which degenerated collagen was extruded [Figure 2] Dermis showed foci of degenerated collagen surrounded by mononuclears, eosinophils and giant cells in irregular palisade arrangement [Figure 3].

 Comments



Perforating GA, a rare variant of GA, may be present along sides of fingers, [5] and this was seen in the present case. Clinically. porokeratosis of Mibelli was excluded as well defined margin did not show groove. Verruca­vulgaris was ruled out histopathologically and clinically. Molluscum-contagiosum was easily differentiated as papules were bigger and central pits rather than punctum were seen. This is perhaps the first case of perforating GA in Indian literature.

References

1Cunliffe WJ . Necrobiotic Disorders. In Textbook of Dermatology (Champion R H, Burton J L, Ebling FJG, eds), 5th edn. London : Blackwell Scientific Publishers, 1992; 2027 - 33.
2Delaney T J, Gold SC, Leppard B. Disseminated perforating granuloma annulare. Brit J Dermatol 1973; 89 : 523-6.
3Owens D W, Freeman R G. Perforating granuloma annulare. Arch Dermatol 1971; 103: 64-7.
4Hazelrigg DE. Generalized perforating granuloma annulare. A case report and review of literature. Cutis 1979; 23: 813-4.
5Dahl MV, Ullman S, Croltz RW. Vasculitis in granuloma annulare. Arch Dermatol 1977; 113: 463-7.

 

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