atypical canine recurrent alopecia
TRANSCRIPT
the recording of the exact location of skin lesions from
different dogs.
We would like to report the development of an open-
source software platform to analyse the punctiform topo-
graphical distribution of canine nodular cutaneous lesions
directly connected with a database that contains clinical,
anamnestic, histopathological, therapeutic and other use-
ful information.
A specific relational Web database for collection of the
characteristics and location of each lesion was created
using open-source software, including the operating sys-
tem (Linux Ubuntu 10.10) MySQL AB version 5.1. A rela-
tional database management system was used to create
the database, and a user-friendly graphical interface was
obtained from the Apache HTTP Server version 2.2 and
Symfony version 1.2.4 (Web application framework writ-
ten in PHP). A Web GIS platform was integrated into the
Web database to allow the registration of topographical
data.1,2
Nodular skin lesions (n = 387) from 350 dogs were
retrieved from the Histopathology Diagnostic Service
of the Department of Food Science, University of
Udine (Italy). A complete dermatological description was
obtained using a multiple-choice format questionnaire to
standardize data collection. The accurate identification of
the topographical location of each lesion was performed
by the clinicians by indicating the lesion on a paper map
drawn of canine mesomorphic breeds. The cutaneous
location of the lesion was inserted into the Web GIS sys-
tem with a GeoTIFF image corresponding to the same
model.
The distribution pattern was analysed by two spatial
statistical methods, i.e. average nearest neighbour and
kernel density function. The results of the nearest neigh-
bour analysis showed a clustering pattern of sites of
onset of lesions examined by query. In particular, the
clustering was evident for the following categories of
nodular lesion: neoplastic (corrected Z-value, �12.04;
P-value <0.001); benign neoplastic (corrected Z-value,
�4.81; P-value <0.001); malignant neoplastic (corrected
Z-value, �4.77; P-value <0.001); and inflammatory lesi-
ons (corrected Z-value, �3.1; P-value <0.01; Figure 1).
Through the kernel density estimation, it was possible to
prepare topographical maps with remarkable clarity. The
maps were easy to interpret, and they showed that the
highest relative density of all nodular lesions (n = 387)
was concentrated on the front part of the animal and in
the scrotal region. The distribution of benign neoplasms
(n = 138) showed maximal values of relative density on
the dorsal portion of the skull. Malignant neoplastic nodu-
lar lesions (n = 139) showed maximal values of relative
density in the topographical area of the chest, the scro-
tum and the posterior surface of the thigh. Inflammatory
nodular lesions (n = 32) showed a strong clustering on
the dorsal surfaces of the metacarpal–phalangeal regionand rostral portion of the dorsal nasal region.
The GIS method used in this study has shown interest-
ing findings. In particular, the use of a GIS system in
mapping lesions could be considered as a new approach
for collection of clinical data from skin lesions.
The creation of density maps of the relative frequency
of nodular skin lesions could be useful for helping veteri-
nary clinicians to have a general idea about the possible
differential diagnoses when presented with such lesions.
This technique could be a valuable aid for training, for
didactic purposes and for researchers. Furthermore, it
allows statistical analysis of nodular skin diseases, includ-
ing, for example, factors such as their anatomical distribu-
tion, breed association and disease incidence.
Sources of Funding
This study was self-funded.
Conflict of Interest
No conflicts of interest have been declared.
Ernesto Pascotto*, Paolo Tom�e*, Stefano Comazzi†,Galeotti Marco* and Luisa Cornegliani†
*Dipartimento di Scienze degli Alimenti, University of
Udine, via Sondrio 2/a, 33100 Udine, Italy
†Dipartimento di Scienze Veterinarie e Sanit�a Pubblica,
University of Milan, via Celoria 20, 10100 Milano, Italy
References
1. Burrough PA. Principles of Geographical Information Systems for
Land Resource Assessment. Oxford, UK: Clarendon Press, 1986.
2. Pfeiffer DU, Robinson TP, Stevenson M et al. Spatial Analysis in
Epidemiology. Oxford, UK: Oxford University Press, 2008.
DOI: 10.1111/vde.12097
Atypical canine recurrent alopecia
We would like to describe an unusual case of seasonal
recurrent alopecia.
The current literature describes recurrent flank alopecia
as a noninflammatory alopecia of the thoracolumbar area
sometimes in conjunction with the dorsal muzzle, base of
the ears, base of the tail and perineum.1,2 The unique
features of this disease are that it is recurrent in most
cases in the same period of the year and that spontane-
ous regrowth is seen.
A 5-year-old intact male cane corso dog was presented
for the complaint of recurrent episodes of alopecia.
Historically, for three consecutive years the dog had
Correspondence: Sophie I. J. Vandenabeele, Department of Small
Animal Medicine and Clinical Biology, Faculty of Veterinary Medicine,
Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium.
E-mail: [email protected]
© 2013 ESVD and ACVD, Veterinary Dermatology, 25, 55–60.56
Letter to the Editor
developed alopecia on the face in March or April with
spontaneous regrowth in July. The first episode started in
March at 2 years of age, at which time investigation was
declined by the owner. The dog was presented again
2 years later in March at the beginning of the third epi-
sode of alopecia. The only abnormalities found on exami-
nation were related to the skin. The dermatological
examination revealed complete alopecia of the dorsal
muzzle, facial folds and convex and concave sides of both
pinnae (Figure 1). The presence of hyperpigmentation in
the affected areas was hard to assess due to an already
heavily pigmented skin. Mild ear margin hyperkeratosis
was also present. The remaining hair coat was normal;
there was no alopecia or difference in coat colour or tex-
ture of the hair on the dog’s lateral flank area.
A serum biochemistry panel, complete blood count and
basal thyroxin and thyroid-stimulating hormone levels
were within laboratory normal limits. A trichogram did not
show melanin clumping or fractured hair shafts. Two
8 mm skin biopsy tissue samples were taken from the
alopecic area on the dorsal muzzle and one 8 mm skin
biopsy tissue sample from the facial fold. Histopathologi-
cal findings were similar in all three samples. A uniform
melanosis of the epidermis was noted. The hair follicles
demonstrated hair cycle arrest, being in catagen or telo-
gen phase. There was marked infundibular hyperkeratosis
extending to the secondary hair follicles. In addition, there
was mild follicular dysplasia. Some perifollicular pigmen-
tary incontinence was noted. The sebaceous glands were
melanized (Figure 2). Hair shafts were normal. Given the
cyclical occurrence of the alopecia and the spontaneous
regrowth, combined with the histopathology features, a
diagnosis of an atypical presentation of recurrent flank
alopecia was made. The owner elected not to treat the
dog.
We have seen a similar clinical presentation in several
dogues de Bordeaux dogs with noninflammatory sea-
sonal alopecia limited to the dorsal muzzle, facial folds
and pinnae with spontaneous regrowth, which we sus-
pect to be the same, but unfortunately the owners did
not allow skin biopsy in those cases. Although hypothy-
roidism can present with alopecia on the bridge of the
nose due to friction, hair does not regrow spontaneously
in dogs with hypothyroidism.2
Other differential diagnoses included black hair follicu-
lar dysplasia and noncolour-linked follicular dysplasia.
Both of these dysplastic diseases evolve into a progres-
sive and more permanent alopecia, which was not seen
in this dog.3–5 Moreover, both the distribution of the
lesions and the cyclical episodes of alopecia and hair
regrowth do not fit with the description of black hair
follicular dysplasia and noncolour-linked dysplasia.
In conclusion, we report a case with an atypical facial
distribution of lesions of canine recurrent alopecia, with-
out involvement of the flanks.
Sources of Funding
This study was self-funded.
Conflict of Interest
No conflicts of interest have been declared.
Sophie I. J. Vandenabeele*, Jan Declercq*, Sylvie
Daminet*, Ilona Schwarzkopf† and Hilde E. V. De Cock‡*Department of Small Animal Medicine and Clinical
Biology, Faculty of Veterinary Medicine, Ghent University,
Salisburylaan 133, B-9820 Merelbeke, Belgium
†DACMalpertuus, B-9070 Heusden, Belgium
‡Veterinary Pathology Services/Medvet, B-2020
Antwerpen, Belgium
References
1. Miller WH, Griffin CE, Campbell LC. Miscellaneous alopecias. In:
Muller and Kirk’s Small Animal Dermatology. 7th edition. St Louis,
MO: Elsevier, 2013; 556–559.
2. Paradis M. Canine recurrent flank alopecia. In: Mecklenburg L,
Linek M, Tobin DJ eds. Hair Loss Disorders in Domestic Animals.
Ames, IA: Wiley-Blackwell, 2009; 155–160.
Figure 1. Clinical picture demonstrating the striking alopecia of the
dorsal muzzle, supraorbital areas and facial folds.
Figure 2. Histopathology, skin biopsy from the muzzle. Note the hair
cycle arrest, with follicular hyperkeratosis extending to the secondary
follicles, and the melanization of the sebaceous glands (arrowhead).
Haematoxylin and eosin.
© 2013 ESVD and ACVD, Veterinary Dermatology, 25, 55–60. 57
Letter to the Editor
3. Miller WH, Griffin CE, Campbell LC. Congenital and hereditary
defects. In: Muller and Kirk’s Small Animal Dermatology. 7th edi-
tion. St Louis, MO: Elsevier, 2013; 593–597.
4. Gross TL, Ihrke PJ, Walder EJ et al. Dysplastic diseases of the ad-
nexae. In: Skin Diseases of the Dog and Cat: Clinical and Histo-
pathologic Diagnosis. 2nd edition. Oxford: Blackwell Publishing,
2005; 518–522.
5. Cerundolo R, Paradis M, Mecklenburg L. Breed specific canine
hair cycle abnormalities. In: Mecklenburg L, Linek M, Tobin DJ
eds. Hair Loss Disorders in Domestic Animals. Ames, IA:
Wiley-Blackwell, 2009; 169–175.
DOI: 10.1111/vde.12099
‘Cradle cap’ in puppies?
During the second year of her residency in dermatology,
my resident (M. D. Clark, personal communication, 2012)
asked me to look at a 5-week-old healthy male pitbull
dog. Whitish, mildly adherent scale was present on the
skin and in the hair coat over the rump and dorsal trunk.
The skin and hair coat were otherwise normal, and one of
the puppy’s seven littermates – also a male – was like-
wise affected. No diagnostic investigations or treatments
were performed, and the condition spontaneously
resolved over the course of 3 months in both puppies.
Flashback! During the first year of my residency in
medicine, my mentor (R. W. Kirk, personal communica-
tion, 1972) introduced me to my first puppy with what he
called ‘cradle cap’. The puppy was a healthy 6-week-old,
male basenji whose five littermates were unaffected.
White, mildly adherent scale was present on the skin and
in the hair coat over the rump (Figure 1). Areas of the hair
coat – with scale attached to the base of the hairs – were
clumped together and lifting off, revealing normal skin
and regrowing hair coat underneath. Skin scrapings, ace-
tate tape preparations and fungal culture were all nega-
tive. The puppy received no treatment, and the condition
spontaneously resolved over the course of 4 weeks.
Images of another puppy I examined with the identical
presentation in 1980 appear in the 6th edition of Muller &
Kirk’s Small Animal Dermatology (Figs. 14-2 and 14-3).1
This puppy was a healthy 5-week-old female, mixed
breed (Figure 2) whose three littermates were unaf-
fected. No diagnostic investigations or treatments were
performed, and the condition spontaneously resolved by
the time the puppy reached 3 months of age.
To my knowledge, the only reference to this canine
dermatosis appears in the classic textbook of Kr�al and
Schwartzman,2 wherein it is likened to ‘cradle cap’ in
human infants. However, the human condition appears to
be different.3 Adherent, yellow-brown, greasy scales,
crusts and inflammation are present on the scalp. In pup-
pies, greasy adherent scale crust and macroscopic inflam-
mation are not present and the rump is predominantly
affected. Histopathological findings in skin biopsies taken
from infants include spongiotic dermatitis with folliculo-
centric scale crust. Histopathological findings in affected
puppies have not been reported. The conditions are
benign and self-limited in both species.
In puppies, the presentation evokes a differential diag-
nosis of contact dermatitis (chemical or thermal), cheylet-
iellosis and pediculosis. However, no history of a
contactant is gathered, no ectoparasites are found, the
owners have not witnessed a prior dermatitis, and spon-
taneous resolution is the rule. The most useful tests that
might lead us to a better understanding of this condition
would be skin biopsies (for histopathology) and bacterial/
fungal cultures of early lesions. It will be difficult to con-
vince the owners of otherwise healthy puppies with a
Figure 1. Hairs over the rump are clumped together and have adher-
ent whitish scale at the base.
Figure 2. Clumped hairs and whitish scale are present over the
rump.
Correspondence: Danny W. Scott, Department of Clinical Sciences,
College of Veterinary Medicine, Cornell University, Ithaca, NY 14853,
USA. E-mail: [email protected]
© 2013 ESVD and ACVD, Veterinary Dermatology, 25, 55–60.58
Letter to the Editor