utd_medknow
International Journal of Trichology International Journal of Trichology
 Print this page Email this page Small font sizeDefault font sizeIncrease font size
 
 
  Home | About IJT | Editorial board | Search | Ahead of print | Current Issue | Archives | Instructions | Online submission | Subscribe | Advertise | Contact us | Login   
 


 
 Table of Contents  
CASE REPORT
Year : 2018  |  Volume : 10  |  Issue : 2  |  Page : 80-83  

Graft versus host disease presenting as fibrosing alopecia in a pattern distribution: A model for pathophysiological understanding of cicatricial pattern hair loss


1 University Hospital Alvaro Alvim, Campos dos Goytacazes, Brazil
2 Department of Dermatology, Center for Medical Sciences, Fluminense Federal University, University Hospital Antonio Pedro, Niterói, Rio de Janeiro, Brazil
3 Center for Dermatology and Hair Diseases Professor Trüeb, Zurich-Wallisellen, Switzerland

Date of Web Publication23-Apr-2018

Correspondence Address:
Prof. Ralph Michel Trüeb
Center for Dermatology and Hair Diseases Professor Trüeb, Bahnhofplatz 1a, CH-8304 Wallisellen
Switzerland
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijt.ijt_83_17

Rights and Permissions
   Abstract 

A case of cutaneous graft versus host disease (GvHD) presenting as fibrosing alopecia in a pattern distribution (FAPD) is discussed, possibly providing a mechanistic model for a better understanding of the pathogenic events underlying cicatricial pattern hair loss. The implication of a follicular inflammation and fibrosis associated with patterned hair loss has emerged from several independent studies. Eventually, Zinkernagel and Trüeb reported a peculiar type of cicatricial pattern hair loss with histopathological features consistent with lichen planopilaris (LPP) associated with androgenetic alopecia (AGA). With regard to its pathogenesis, LPP is regarded to constitute a T-cell-mediated autoimmune reaction. An as yet unknown antigenic stimulus from the malfunctioning hair follicle may initiate a lichenoid tissue reaction that triggers apoptosis of the follicular epithelial cells in the susceptible individual. GvHD is a complication following allogeneic tissue transplantation and is induced and maintained by immunocompetent cells from the donor tissue that particularly attack epithelia of fast-proliferating tissues in the recipient. Due to its analogies with lichen planus, GvHD constitutes a valid immunologic model for lichen planus, LPP and ultimately FAPD. Specifically, the presentation of GvHD of the scalp combines features of AGA and of LPP, as originally proposed in earlier observations on permanent alopecia after bone marrow transplantation.

Keywords: Cicatricial pattern hair loss, fibrosing alopecia in a pattern distribution, graft versus host disease


How to cite this article:
Rezende HD, Reis Gavazzoni Dias MF, Trüeb RM. Graft versus host disease presenting as fibrosing alopecia in a pattern distribution: A model for pathophysiological understanding of cicatricial pattern hair loss. Int J Trichol 2018;10:80-3

How to cite this URL:
Rezende HD, Reis Gavazzoni Dias MF, Trüeb RM. Graft versus host disease presenting as fibrosing alopecia in a pattern distribution: A model for pathophysiological understanding of cicatricial pattern hair loss. Int J Trichol [serial online] 2018 [cited 2022 Dec 8];10:80-3. Available from: https://www.ijtrichology.com/text.asp?2018/10/2/80/230821


   Introduction Top


Patterned hair loss or androgenetic alopecia (AGA) is understood to represent a hereditary and androgen-sensitive, progressive thinning of the scalp hair. Its pathogenesis is related to a polygenic hereditary background and peculiarities of androgen-metabolism, resulting in androgen-dependent, progressive thinning of hair associated with a decrease of anagen duration in the hair cycle, miniaturization of the hair follicle, and gradual transformation of the terminal to vellus hair in the affected areas.[1] Therefore, diversity of hair shaft diameter [2] or anisotrichosis [3] is a diagnostic dermoscopic feature of AGA. It is best appreciated in a central hair part at low magnification and is very useful to detect the condition, particularly in women.[4]

Treatment of AGA aims at blocking the effect of androgens with antiandrogens, such as cyproterone acetate and spironolactone, or 5 alpha-reductase inhibitors, such as finasteride and dutasteride, and at increasing the duration of anagen with the hair growth-promoting agent minoxidil.[5] The limited success rate of treatment with these agents means that additional pathogenic factors may be considered.

The implication of a follicular inflammation and fibrosis associated with patterned hair loss has emerged from several independent studies: an early study referred to an inflammatory infiltrate of activated T cells and macrophages in the upper third of the hair follicles, associated with an enlargement of the follicular dermal sheath composed of collagen bundles (perifollicular fibrosis) in the regions of actively progressing alopecia.[6] Subsequently, Whiting [7] demonstrated in morphometric studies in patients with male pattern AGA treated with minoxidil that 55% of patients with microinflammation had regrowth in response to treatment, in comparison to 77% in those without inflammation and fibrosis. Ultimately, Mahé et al.[8] proposed the term microinflammation, in as much as the process involves a slow, subtle, and indolent course, in contrast to the inflammatory and destructive process in the classical inflammatory scarring alopecias.

Eventually, Zinkernagel and Trüeb [9] reported a peculiar type of cicatricial pattern hair loss with histopathological features consistent with lichen planopilaris (LPP) associated with AGA and named it fibrosing alopecia in a pattern distribution (FAPD).

With regard to its pathogenesis, LPP is regarded to be a T-cell-mediated autoimmune reaction that triggers apoptosis of the follicular epithelial cells. This autoimmune process is thought to be in response to some antigenic challenge, but a specific antigen has yet not been identified. Harries et al.[10] provide the first evidence that LPP may result from an immune privilege collapse of the hair follicle's epithelial stem cell niche. Where a causal or triggering agent is identified, this is termed a lichenoid reaction rather than lichen planus. This may include drug reactions, viral hepatitis, and cutaneous graft versus host disease (GvHD).

Herein, we report a case of cutaneous GvHD presenting as FAPD, providing a model for a better understanding of the pathogenic mechanisms possibly underlying cicatricial pattern hair loss.


   Case Report Top


A 58-year-old woman presented with the complaint of symptomatic (pruritus) and accelerated hair loss. She had a personal history of acute myeloid leukemia with bone marrow transplantation preceding by 3 years and GvHD of the lung, gut, oral cavity, skin, and nails, that was treated with extracorporeal photopheresis. Her systemic medication consisted of tacrolimus, mycophenolate mofetil, fluconazole, valaciclovir, atovaquone, atorvastatin, sitagliptin, pantoprazole, ramipril, pregabalin, magnesium, calcium, and vitamin D3.

Clinical examination revealed a thinning of hair of the central scalp area [Figure 1] associated with diversity of hair shaft diameters and perifollicular scaling and follicular dropout limited to the respective area on dermoscopic examination [Figure 2]. Associated nail alterations were longitudinal ridges and melanonychia.
Figure 1: Patterned alopecia of the central scalp region

Click here to view
Figure 2: Diversity of hair shaft diameters associated with perifollicular scaling and follicular dropout on dermoscopic examination

Click here to view


A diagnosis of FAPD was made, and the patient was prescribed a compound of 5% minoxidil and 0.2% triamcinolone acetonide b. i. d. for the crown area.


   Discussion Top


Cicatricial pattern hair loss is the term proposed by Olsen [11] in 2005 to acknowledge the existence of follicular inflammatory phenomena and fibrosis with follicular dropout in biopsies of women with AGA.

In 1994, Kossard [12] originally reported on scarring alopecia in a pattern distribution in postmenopausal women with progressive frontal hairline recession that was associated with perifollicular erythema within the marginal hairline, producing a frontal fibrosing alopecia extending to the temporal and parietal hair margins. Scalp biopsy specimens revealed histological features that were indistinguishable from those seen in LPP.[13] FFA has meanwhile also been described in premenopausal women and men [14],[15],[16],[17],[18] though with a significantly lesser frequency. Moreover, it has been recognized to represent a more generalized rather than localized process of inflammatory scarring alopecia, with extension well beyond the frontotemporal hairline to include the parieto-occipital hair line, involve peculiar facial papules as evidence of facial vellus hair involvement,[19] and loss of peripheral body hair.[20],[21] More recently, also lichen planus-type nail involvement has been reported,[22] again pointing to a close relationship of FFA to lichen planus. It has been speculated to what extent a background of AGA may contribute to this particular clinical presentation of the disease, specifically in patients suffering of lupus erythematosus presenting with FFA.[23] Nevertheless, the localization of FFA in androgen-independent areas, the lack of evidence of associated AGA (diversity of hair shaft diameters) in some patients with FFA, and the limited success rate of antiandrogen therapy, including 5 alpha-reductase inhibitors, all point to the fact that AGA represents only a facultative comorbidity of FFA, setting the condition apart from FAPD.

An important question that arises is how the lichenoid tissue reaction pattern is generated around the individual androgenetic hair follicle in FAPD. Follicles with some form of damage or malfunction might express cytokine profiles that attract inflammatory cells to assist in damage repair or in the initiation of apoptosis-mediated organ deletion. Alternatively, an as yet unknown antigenic stimulus from the damaged or malfunctioning hair follicle might initiate a lichenoid tissue reaction in the immunogenetically susceptible individual. Remarkably, in healthy murine skin, clusters of perifollicular macrophages have been described as perhaps indicating the existence of a physiological program of immunologically controlled hair follicle degeneration by which malfunctioning follicles are removed by programmed organ deletion.[24] It has therefore been proposed that various forms of clinically perceptible, permanent alopecia might represent a pathological exaggeration of this type of programmed organ deletion,[24] resulting in a lichenoid tissue reaction pattern and true scarring alopecia. Further studies are required to elucidate a presumable role of androgenetic factors in addition to that of the lymphohistiocytic infiltrate, perifollicular lamellar fibrosis, and apoptosis-mediated follicular regression in FAPD.

GvHD is a common complication following allogeneic tissue transplantation and is induced and maintained by immunocompetent cells from the donor tissue (graft) that particularly attack epithelia of fast proliferating tissues in the recipient (host), such as those from the gastrointestinal tract, liver, and the skin. The skin is the most common organ involved. While the cutaneous, mucosal, and nail manifestations of chronic GvHD are well recognized, involvement of the hair follicle has so far found lesser attention. Miyazaki et al.[25] reported the first case of GvHD with follicular involvement.

Due to its analogies with lichen planus, GvHD constitutes a model that may lead to a better understanding of the pathophysiological features of lichen planus, LPP, and ultimately FAPD. Specifically, the presentation of chronic GvHD on the scalp may be that of FAPD with features of both AGA and of LPP, as originally proposed by Basilio et al.[26] in their earlier observations on permanent alopecia after bone marrow transplantation.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understand that name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

This case report represents an integral part of Hudson Dutra Rezende's traineeship in Dermato-Trichology at the Center for Dermatology and Hair Diseases Professor Trüeb.

 
   References Top

1.
Paus R, Cotsarelis G. The biology of hair follicles. N Engl J Med 1999;341:491-7.  Back to cited text no. 1
[PUBMED]    
2.
de Lacharrière O, Deloche C, Misciali C, Piraccini BM, Vincenzi C, Bastien P, et al. Hair diameter diversity: A clinical sign reflecting the follicle miniaturization. Arch Dermatol 2001;137:641-6.  Back to cited text no. 2
    
3.
Sewell LD, Elston DM, Dorion RP. “Anisotrichosis”: A novel term to describe pattern alopecia. J Am Acad Dermatol 2007;56:856.  Back to cited text no. 3
[PUBMED]    
4.
Galliker NA, Trüeb RM. Value of trichoscopy versus trichogram for diagnosis of female androgenetic alopecia. Int J Trichology 2012;4:19-22.  Back to cited text no. 4
    
5.
Price VH. Treatment of hair loss. N Engl J Med 1999;341:964-73.  Back to cited text no. 5
[PUBMED]    
6.
Jaworsky C, Kligman AM, Murphy GF. Characterization of inflammatory infiltrates in male pattern alopecia: Implications for pathogenesis. Br J Dermatol 1992;127:239-46.  Back to cited text no. 6
[PUBMED]    
7.
Whiting DA. Diagnostic and predictive value of horizontal sections of scalp biopsy specimens in male pattern androgenetic alopecia. J Am Acad Dermatol 1993;28:755-63.  Back to cited text no. 7
[PUBMED]    
8.
Mahé YF, Michelet JF, Billoni N, Jarrousse F, Buan B, Commo S, et al. Androgenetic alopecia and microinflammation. Int J Dermatol 2000;39:576-84.  Back to cited text no. 8
    
9.
Zinkernagel MS, Trüeb RM. Fibrosing alopecia in a pattern distribution: Patterned lichen planopilaris or androgenetic alopecia with a lichenoid tissue reaction pattern? Arch Dermatol 2000;136:205-11.  Back to cited text no. 9
    
10.
Harries MJ, Meyer K, Chaudhry I, E Kloepper J, Poblet E, Griffiths CE, et al. Lichen planopilaris is characterized by immune privilege collapse of the hair follicle's epithelial stem cell niche. J Pathol 2013;231:236-47.  Back to cited text no. 10
[PUBMED]    
11.
Olsen EA. Female pattern hair loss and its relationship to permanent/cicatricial alopecia: A new perspective. J Investig Dermatol Symp Proc 2005;10:217-21.  Back to cited text no. 11
[PUBMED]    
12.
Kossard S. Postmenopausal frontal fibrosing alopecia. Scarring alopecia in a pattern distribution. Arch Dermatol 1994;130:770-4.  Back to cited text no. 12
[PUBMED]    
13.
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. 13
[PUBMED]    
14.
Samrao A, Chew AL, Price V. Frontal fibrosing alopecia: A clinical review of 36 patients. Br J Dermatol 2010;163:1296-300.  Back to cited text no. 14
[PUBMED]    
15.
MacDonald A, Clark C, Holmes S. Frontal fibrosing alopecia: A review of 60 cases. J Am Acad Dermatol 2012;67:955-61.  Back to cited text no. 15
[PUBMED]    
16.
Ladizinski B, Bazakas A, Selim MA, Olsen EA. Frontal fibrosing alopecia: A retrospective review of 19 patients seen at duke university. J Am Acad Dermatol 2013;68:749-55.  Back to cited text no. 16
[PUBMED]    
17.
Banka N, Mubki T, Bunagan MJ, McElwee K, Shapiro J. Frontal fibrosing alopecia: A retrospective clinical review of 62 patients with treatment outcome and long-term follow-up. Int J Dermatol 2014;53:1324-30.  Back to cited text no. 17
[PUBMED]    
18.
Vañó-Galván S, Molina-Ruiz AM, Serrano-Falcón C, Arias-Santiago S, Rodrigues-Barata AR, Garnacho-Saucedo G, et al. Frontal fibrosing alopecia: A multicenter review of 355 patients. J Am Acad Dermatol 2014;70:670-8.  Back to cited text no. 18
    
19.
Donati A, Molina L, Doche I, Valente NS, Romiti R. Facial papules in frontal fibrosing alopecia: Evidence of vellus follicle involvement. Arch Dermatol 2011;147:1424-7.  Back to cited text no. 19
[PUBMED]    
20.
Armenores P, Shirato K, Reid C, Sidhu S. Frontal fibrosing alopecia associated with generalized hair loss. Australas J Dermatol 2010;51:183-5.  Back to cited text no. 20
[PUBMED]    
21.
Chew AL, Bashir SJ, Wain EM, Fenton DA, Stefanato CM. Expanding the spectrum of frontal fibrosing alopecia: A unifying concept. J Am Acad Dermatol 2010;63:653-60.  Back to cited text no. 21
[PUBMED]    
22.
Macpherson M, Hohendorf-Ansari P, Trüeb RM. Nail involvement in frontal fibrosing alopecia. Int J Trichology 2015;7:64-6.  Back to cited text no. 22
    
23.
Gaffney DC, Sinclair RD, Yong-Gee S. Discoid lupus alopecia complicated by frontal fibrosing alopecia on a background of androgenetic alopecia. Br J Dermatol 2013;169:217-8.  Back to cited text no. 23
[PUBMED]    
24.
Eichmüller S, van der Veen C, Moll I, Hermes B, Hofmann U, Müller-Röver S, et al. Clusters of perifollicular macrophages in normal murine skin: Physiological degeneration of selected hair follicles by programmed organ deletion. J Histochem Cytochem 1998;46:361-70.  Back to cited text no. 24
    
25.
Miyazaki K, Higaki S, Maruyama T, Takahashi S, Morohashi M, Ito K, et al. Chronic graft-versus-host disease with follicular involvement. J Dermatol 1993;20:242-6.  Back to cited text no. 25
    
26.
Basilio FM, Brenner FM, Werner B, Rastelli GJ. Clinical and histological study of permanent alopecia after bone marrow transplantation. An Bras Dermatol 2015;90:814-21.  Back to cited text no. 26
[PUBMED]    


    Figures

  [Figure 1], [Figure 2]


This article has been cited by
1 Fibrosing alopecia in a pattern distribution
Jacob Griggs, Ralph M. Trüeb, Maria Fernanda Reis Gavazzoni Dias, Maria Hordinsky, Antonella Tosti
Journal of the American Academy of Dermatology. 2021; 85(6): 1557
[Pubmed] | [DOI]
2 Early recognition of chronic rejection in a face allotransplant patient with alopecia
Neslihan Akdogan, Sibel Ersoy-Evans, Ozay Gokoz, Yunus Erdem, Serdar Nasir
Journal of Cutaneous Pathology. 2021; 48(10): 1286
[Pubmed] | [DOI]
3 Comment on: folliculitis decalvans and lichen planopilaris phenotypic spectrum: a case report of two paediatric cases
R.M. Trüeb
Journal of the European Academy of Dermatology and Venereology. 2021; 35(12)
[Pubmed] | [DOI]
4 Focal and diffuse fibrosing alopecias: Classical lichen planopilaris, frontal fibrosing alopecia, fibrosing alopecia with a pattern distribution, cicatricial pattern hair loss, and lichen planopilaris diffuse pattern
Xufeng Du, Yuqian Li, Qilin Zhu, Jing Zhu, Wengrong Xu, Zhongming Li, Dirk M. Elston
JAAD Case Reports. 2020; 6(5): 403
[Pubmed] | [DOI]
5 Acute Hair Loss 3 Years after Bone Marrow Transplant
Laura Silva, Maria Natália De Fraia Souza, Solange Teixeira, Flavia Sternberg, Juliana Dumet Fernandes
Skin Appendage Disorders. 2019; 5(4): 255
[Pubmed] | [DOI]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
   Case Report
   Discussion
    References
    Article Figures

 Article Access Statistics
    Viewed3820    
    Printed113    
    Emailed0    
    PDF Downloaded28    
    Comments [Add]    
    Cited by others 5    

Recommend this journal