Diagnosis
of alopecia areata
Alopecia areata is a non-scarring, inflammatory, hair loss
disease that is seen in men, women and children. This condition
is commonly manifested by patchy areas of complete hair loss on
the scalp and other body parts. In severe cases, alopecia areata
can progress to complete loss of all body hair. While not a life
threatening condition, alopecia areata nonetheless has serious
implications for the victim and family members because of its
psychological and sociological backlash.
Although great progress has been made in the research of hair
diseases, the exact etiology of alopecia areata is still
to be established. However, there is a lot of evidence to support
the fact that alopecia areata is a multi-entity disorder with
causes that are multifactorial, including evident autoimmune and
genetic components. The disease presents with the loss of scalp
and body hair by interruption of their synthesis. There is no
destruction or atrophy of the follicles, and therefore the hair
loss can be reversible.
Normally, hair growth in each hair follicle occurs in a cycle.
There are three main phases of the hair growth cycle anagen (active
growth phase), catagen (period of controlled regression) and telogen
(resting state in the hair follicle cycle). Alopecia areata primarily
affects the hair follicle as it enters the anagen phase, and studies
further indicate that the initial event in the development of
alopecia areata is the premature precipitation of anagen follicles
into the telogen state or resting state of the hair follicle cycle.
There is currently no conclusive diagnostic test for alopecia
areata Dermatologists deduce alopecia areata by a process of elimination
of other hair loss causes and close examination of the lesion itself.
Typically, the initial alopecia areata lesion appears as a smooth
bald patch sometimes within 24 hours. Some people feel a tingling
sensation or pain in the affected area. The scalp is the most commonly
affected area but alopecia areata can present in any region of hair
on the body. Hair pull tests are sometimes conducted at the margins
of lesions. If hair is easily pulled out, it is indicative that
the lesion is active and further hair loss should be anticipated.
The hair fiber that falls out in alopecia areata has been the
subject of several analytical studies and is sometimes used to diagnose
alopecia areata. Using scanning electron microscopy the hair fibers
falling out from the edge of an expanding bald patch can look very
unusual. Frequently, the part of the hair fiber furthest away from
the scalp (the oldest part of the hair) looks normal. Closer to
the scalp (newer part of the hair) and it can look quite aberrant.
We find the shape of the fiber becomes increasingly irregular the
closer to the scalp we look. This involves deposits of unordered
keratin and constrictions in the hair fiber. The cuticle can be
missing and there can be longitudinal cracks along the length of
the hair. Analysis of the hair fiber shows the constituent keratins
to remain the same but the way they are assembled to make up the
fiber becomes increasingly abnormal.
The irregular construction of the hair gives it weak spots where
it can readily break off. This gives rise to the stumpy hair fibers
called exclamation mark hairs that can often be seen in expanding
patches of alopecia areata. The hairs are so called because they
look like an exclamation mark [!]. Some dermatologists use presence
of exclamation mark hairs as diagnostic for alopecia areata. However,
it has been shown that exclamation mark hairs can occasionally occur
in other conditions as well.
Anywhere between 7% and 66% of people with alopecia areata also
have aberrant nail formation depending on which reports you read
(Muller 1963, Baran 1984). It is generally agreed that 25% is a
more realistic figure (around the mid point between 7% and 66%).
Disruption of growth may involve all or just one of the nails. Nail
dystrophy varies from a diffuse, fine pitting to severe alteration
in a few cases (Gollinck 1990).
For a more definitive diagnosis, dermatologists sometimes need
to take a small skin biopsy (a small piece of skin about 4mm in
diameter) for microscopic examination. With this, dermatologists
can see whether there is focal inflammation of the hair follicles.
This is the clearest method of identifying alopecia areata. More
recently it has been suggested that a blood samples could be tested
for the presence of hair follicle specific autoantibodies. However,
while this is possible to do in a research or pathology laboratory
no standardized test has been developed for the general dermatology
clinic.
Diagnosis
of alopecia areata references
- Nunez J,
Grande K, Hsu S. Alopecia areata with features of loose anagen
hair. Pediatr Dermatol. 1999 Nov-Dec;16(6):460-2.
- Kim IH,
Jo HY, Cho CG, Choi HC, Oh CH. Quantitative image analysis of
hair follicles in alopecia areata. Acta Derm Venereol. 1999 May;79(3):214-6.
- Hoss DM,
Grant-Kels JM. Diagnosis: alopecia areata or not? Semin Cutan
Med Surg. 1999 Mar;18(1):84-90.
- Kossard
S. Diffuse alopecia with stem cell folliculitis: chronic diffuse
alopecia areata or a distinct entity? Am J Dermatopathol. 1999
Feb;21(1):46-50.
- Tobin SJ.
Morphological analysis of hair follicles in alopecia areata. Microsc
Res Tech. 1997 Aug 15;38(4):443-51.
- Elston
DM, McCollough ML, Bergfeld WF, Liranzo MO, Heibel M. Eosinophils
in fibrous tracts and near hair bulbs: a helpful diagnostic feature
of alopecia areata. J Am Acad Dermatol. 1997 Jul;37(1):101-6.
- Tobin DJ,
Orentreich N, Fenton DA, Bystryn JC. Antibodies to hair follicles
in alopecia areata. J Invest Dermatol. 1994 May;102(5):721-4.
- Peereboom-Wynia
JD, Beek CH, Mulder PG, Stolz E. The trichogram as a prognostic
tool in alopecia areata. Acta Derm Venereol. 1993 Aug;73(4):280-2.
- Ihm CW,
Han JH. Diagnostic value of exclamation mark hairs. Dermatology.
1993;186(2):99-102.
- Hatzis
J, Kostakis P, Tosca A, Parissis N, Nicolis G, Varelzidis A, Stratigos
J. Nuchal nevus flammeus as a skin marker of prognosis in alopecia
areata. Dermatologica. 1988;177(3):149-51.
- El Darouti M, Marzouk SA, Sharawi E. Eosinophils
in fibrous tracts and near hair bulbs: A helpful diagnostic feature
of alopecia areata. J Am Acad Dermatol. 2000 Feb;42(2 Pt 1):305-7.
- Tosti A, Piraccini BM, Alagna G. Temporary
hair loss simulating alopecia areata after endovascular surgery
of cerebral arteriovenous malformations: a report of 3 cases.
Arch Dermatol. 1999 Dec;135(12):1555-6
- Bauer A. [Isolated falling out of upper
eyelid hair]. Dtsch Med Wochenschr. 1999 Jun 11;124(23):747.
- Shapiro J, Madani S. Alopecia areata: diagnosis
and management. Int J Dermatol. 1999 May;38 Suppl 1:19-24.
- Hoffmann R, Happle R. [Alopecia areata.
1: Clinical aspects, etiology, pathogenesis]. Hautarzt. 1999 Mar;50(3):W222-31.
- Verraes S, Vereecken P. [Alopecia areata:
diagnostic and therapeutic approach]. Rev Med Brux. 1997 Dec;18(6):389-93.
- Carson HJ, Pellettiere EV, Lack E. Alopecia
neoplastica simulating alopecia areata and antedating the detection
of primary breast carcinoma. J Cutan Pathol. 1994 Feb;21(1):67-70.
- Jackson D, Church RE, Ebling FJ.Alopecia
areata hairs: a scanning electron microscope study. Br J Dermatol.
1971 Sep;85(3):242-6.
- Goos M. [The histopathology of alopecia
areata. With special reference to the duration, location and progession
of hair loss]. Arch Dermatol Forsch. 1971;240(2):160-72.
- Shelley WB. Letter: Triangular hair patch
as sign of alopecia areata. Arch Dermatol. 1974 Jan;109(1):102.
- Lazovic-Tepavac O, Salamon T. [Histopathology
of alopecia areata]. Dermatol Monatsschr. 1970 Jul;156(7):665-75.
- Shuster S. 'Coudability': a new physical
sign of alopecia areata. Br J Dermatol. 1984 Nov;111(5):629.
- Tobin DJ, Fenton DA, Kendall MD. Transient
defects in cortical cell differentiation form the exclamation-mark
shaft in acute alopecia areata. Ann N Y Acad Sci. 1991 Dec 26;642:483-6.
- Keipert JA. The most common type of fractured
hair in alopecia areata in children: another cause of "black dot
disease". Australas J Dermatol. 1978 Aug;19(2):74-5.
- Muller SA, Winkelmann RK. Alopecia areata.
An evaluation of 736 patients. Arch Dermatol 1963; 88: 290-297.
- Baran R, Dawber RPR. Diseases of the nails
and their management. Oxford, Blackwell Scientific Publications,
1984.
- Gollinck H, Orfanos CE. Alopecia areata:
pathogenesis and clinical picture. In: Hair and Hair Diseases
(Orfanos CE, Happle R, eds), Berlin, Springer-Verlag, 1990; 529-569.
|