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Year : 2016  |  Volume : 8  |  Issue : 4  |  Page : 173-175  

Graham–Little–Piccardi syndrome: A lens through beyond what is known

1 Department of Dermatology, Rita Skin Foundation, Kolkata, West Bengal, India
2 Department of Dermatology, Burdwan Medical College and Hospital, Burdwan, West Bengal, India
3 Department of Dermatology, KPC Medical College, Kolkata, West Bengal, India
4 Postgraduate Institute of Medical Education and Research, Kolkata, West Bengal, India

Date of Web Publication28-Mar-2017

Correspondence Address:
Abhijit Saha
Flat No. 115, 1st Floor, Block B, Rishav Palace, 77/26 Ram Lal Dutta Lane, Bhadrakali, Uttarpara, Hooghly - 712 232, West Bengal
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0974-7753.203180

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Graham–Little–Piccardi syndrome (GLPS) is a rare form of follicular lichen planus and comprises cicatricial alopecia of the scalp, noncicatricial alopecia of the axillae, and/or pubis and spinous follicular papules involving the trunk and extremities. We herein report a classic case of GLPS in a 49-year-old female. Uniqueness of our case is due to its additional features of frontal fibrosing alopecia (FFA). Although overlap between GLPS and FFA has been mentioned in literature, such numbers are scanty. Therapeutic response with oral steroid and retinoid is also far better in contrast to what is described in the existing literature.

Keywords: Follicular lichen planus, frontal fibrosing alopecia, therapeutic response

How to cite this article:
Saha A, Seth J, Das A, Dhar S. Graham–Little–Piccardi syndrome: A lens through beyond what is known. Int J Trichol 2016;8:173-5

How to cite this URL:
Saha A, Seth J, Das A, Dhar S. Graham–Little–Piccardi syndrome: A lens through beyond what is known. Int J Trichol [serial online] 2016 [cited 2022 Dec 5];8:173-5. Available from: https://www.ijtrichology.com/text.asp?2016/8/4/173/203180

   Introduction Top

Frontal fibrosing alopecia (FFA) is increasingly considered as a distinct variant of lichen planopilaris (LPP), with scarring alopecia of frontotemporal hairline and nonscarring alopecia of the eyebrows. FFA and Graham–Little–Piccardi syndrome (GLPS) can be considered as spectrum of a disease as per the current literature [1] due to the presence of overlapping features. Coexistence of these two uncommon presentations has rarely been reported in scientific literature.

   Case Report Top

A 49-year-old female presented with hair loss from both center and sides of the scalp for the last 1 year which did not improve following minoxidil therapy. She also complained of generalized pruritus and gritty sensation all over the body. She had completed her family gracefully with two healthy children. Her family history was unremarkable, and she did not suffer from any chronic disease. No history of chronic medication could be elicited. Personal and family history of photosensitivity was absent.

On examination, we found scarring alopecia with follicular papules and mild scaling over the vertex [Figure 1]a and [Figure 1]b. She had definite recession of frontotemporal hairline with bilaterally symmetrical band-like scarring alopecia of the same region [Figure 2]. There were numerous violaceous follicular spinous papules distributed over the abdomen, back, arms, and legs [Figure 3]a,[Figure 3]b,[Figure 3]c. Her palms, soles, nail, and oral mucosa were not involved. Further examination revealed nonscarring alopecia over the axillae and pubis [Figure 4]. She did not allow us to take photograph of the pubic area.
Figure 1: (a) Scarring alopecia with follicular papules and mild scaling over the vertex. (b) Close-up view

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Figure 2: Recession of frontotemporal hairline with symmetrical band-like scarring alopecia

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Figure 3: (a) Violaceous follicular spinous papules over the abdomen. (b) Violaceous follicular spinous papules over the back. (c) Violaceous follicular spinous papules over the leg

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Figure 4: Nonscarring alopecia over the axilla

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Routine investigations with complete hemogram, blood sugar, liver function test including hepatitis profile and thyroid screening were within normal limit. Histopathological examination from scalp biopsy revealed hyperkeratotic epidermis with acanthosis and follicular plugging. There was definite basal cell degeneration with band-like chronic inflammatory infiltrate around perifollicular region. Dermis showed occasional loss of hair follicle and perifollicular fibrosis. All these features were consistent with LPP [Figure 5]a and [Figure 5]b.
Figure 5: (a) Follicular plugging with band-like chronic inflammatory infiltrate around perifollicular region, occasional loss of hair follicles, and perifollicular fibrosis (H and E, ×10). (b) Follicular plugging with definite basal cell degeneration with band-like chronic inflammatory infiltrate around perifollicular region (H and E, ×40)

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Based on above findings, a diagnosis of GLPS with FFA was made, and the patient was put on oral prednisolone (1 mg/kg/day) and oral retinoid (0.5 mg/kg/day) for initial 2 weeks. Dose of the steroid was tapered to 20 mg/day and continued along with the same dose of oral isotretinoin (20 mg) for another 2 weeks with strict monitoring of blood parameters without any alteration. At the end of 1 month, the patient had significant improvement of pruritus and hair loss with flattening of the follicular papules. Doses of steroid and isotretinoin were further reduced to 10 mg/day and 15 mg/day, respectively, for another 1 month with further flattening of follicular papules and improvement of FFA patch. Now, the patient is on only 15 mg oral retinoid every alternate day and with regular follow-up on a monthly basis. Follicular papules almost resolved with residual postinflammatory hyperpigmentation [Figure 6]a and [Figure 6]b.
Figure 6: (a) Flattening of follicular papules with residual postinflammatory hyperpigmentation following treatment. (b) Posttherapy improvement of frontal fibrosing alopecia patch

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   Discussion Top

The entity, GLPS was born with a lot of controversies as far as proper clinical definition is concerned.[2],[3] Our observation of simultaneous presence of two variants may further add fire to the unsolved issues of this strange entity.

GLPS is an unusual variant of LPP characterized by multifocal cicatricial alopecia of the scalp, noncicatricial alopecia of the axillae, and/or pubis and follicular lichen planus (LP) involving the trunk and extremities. On the other hand, FFA is increasingly recognized as a distinct variant of LPP in recent years.[4] This progressive form of fibrosing alopecia has failed to show any significant difference from other forms of LPP as far as histopathology and immunophenotyping are concerned.[5],[6] Only differentiating point is symmetrical distribution and predilection for frontotemporal and parietal regions. If we look into the pathogenesis, GLPS is generally considered of having an autoimmune origin.[2],[7] In FFA, the lymphocytic infiltrate and fibrosis affect selectively the intermediate and the vellus-like follicles of the frontal margin and eyebrows. Although the reason for this selective involvement is still an enigma, it is hypothesized that it may represent a variety of LPP with selective involvement of certain androgen-dependent areas. The affected follicles may have typical biologic markers that could explain typical characteristic feature of FFA.[8]

There was several existing literatures where FFA was found to be associated with different forms of LP. In one report, authors concluded FFA as a phenotypic variation of GLPS where additional features are nonscarring alopecia of the eyebrow and axillae and follicular LP over the face.[1] Other authors described FFA in the association of cutaneous LP [9] and oral mucosal LP.[6] To the best of our knowledge, like our case, no such case has been reported till date where FFA is found along with full blown GLPS with all features.

There are several treatment options available for LPP such as oral steroid, oral retinoid, cyclosporine, mycophenolate mofetil, hydroxychloroquine, and psoralen plus ultraviolet A therapy. Most of the recent and existing literatures say that treatment is difficult and challenging.[10],[11],[12] Surprisingly, our case responded very well in terms of symptomatic improvement, clearing of lesions, and halt of progressive alopecia.

   Conclusion Top

The classical and extensive presentation of GLPS along with concomitant FFA in the index case portrays a rare and unique presentation of follicular LP. Such a coexistence of these two variants of LPP may be a mere overlap, a phenotypic variation of the same entity, or it may help in future to frame a newer nosology for LPP.

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


Conflicts of interest

There are no conflicts of interest.

   References Top

Abbas O, Chedraoui A, Ghosn S. Frontal fibrosing alopecia presenting with components of Piccardi-Lassueur-Graham-Little syndrome. J Am Acad Dermatol 2007;57 2 Suppl: S15-8.  Back to cited text no. 1
Vashi N, Newlove T, Chu J, Patel R, Stein J. Graham-Little-Piccardi-Lassueur syndrome. Dermatol Online J 2011;17:30.  Back to cited text no. 2
Matta M, Kibbi AG, Khattar J, Salman SM, Zaynoun ST. Lichen planopilaris: A clinicopathologic study. J Am Acad Dermatol 1990;22:594-8.  Back to cited text no. 3
Dawn G, Holmes SC, Moffat D, Munro CS. Post-menopausal frontal fibrosing alopecia. Clin Exp Dermatol 2003;28:43-5.  Back to cited text no. 4
Kossard S, Lee MS, Wilkinson B. Postmenopausal frontal fibrosing alopecia: A frontal variant of lichen planopilaris. J Am Acad Dermatol 1997;36:59-66.  Back to cited text no. 5
Trüeb RM, Torricelli R. Lichen planopilaris simulating postmenopausal frontal fibrosing alopecia (Kossard). Hautarzt 1998;49:388-91.  Back to cited text no. 6
Pai VV, Kikkeri NN, Sori T, Dinesh U. Graham-Little Piccardi Lassueur syndrome: An unusual variant of follicular lichen planus. Int J Trichology 2011;3:28-30.  Back to cited text no. 7
Tosti A, Piraccini BM, Iorizzo M, Misciali C. Frontal fibrosing alopecia in postmenopausal women. J Am Acad Dermatol 2005;52:55-60.  Back to cited text no. 8
Faulkner CF, Wilson NJ, Jones SK. Frontal fibrosing alopecia associated with cutaneous lichen planus in a premenopausal woman. Australas J Dermatol 2002;43:65-7.  Back to cited text no. 9
Srivastava M, Mikkilineni R, Konstadt J. Lassueur-Graham-Little-Piccardi syndrome. Dermatol Online J 2007;13:12.  Back to cited text no. 10
Assouly P, Reygagne P. Lichen planopilaris: Update on diagnosis and treatment. Semin Cutan Med Surg 2009;28:3-10.  Back to cited text no. 11
Baibergenova A, Donovan J. Lichen planopilaris: Update on pathogenesis and treatment. Skinmed 2013;11:161-5.  Back to cited text no. 12


  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]

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