clinical resolution of nasal aspergillosis following therapy with a homeopathic remedy in a dog
TRANSCRIPT
CASE REPORTS
Clinical Resolution of Nasal AspergillosisFollowing Therapy with a HomeopathicRemedy in a DogShelley Epstein, VMD, Robert Hardy, DVM, MS, DACVIM
ABSTRACTA 6 yr old, male, neutered Weimaraner was treated homeopathically for nasal aspergillosis after failing to respond to two
treatments of topical (intranasal) clotrimazole and oral amoxicillin trihydrate/clavulanate potassium. Computed tomography,
rhinoscopy, fungal culture, and cytology previously confirmed the diagnosis. At presentation for homeopathic treatment, the
dog had aggressive left-sided sinusitis and rhinitis with destruction of nasal turbinates and severe bouts of epistaxis. Erosion
and depigmentation of the nasal planum were evident. After two treatments with homeopathic aurummetallicum, resolution of
clinical signs occurred and clearance of the aspergillosis organisms was documented by computed tomographic scan, rhi-
noscopy, and histopathology. Homeopathic aurummetallicummay be beneficial in treating cases of canine nasal aspergillosis.
(J Am Anim Hosp Assoc 2011; 47:e110–e115. DOI 10.5326/JAAHA-MS-5560)
IntroductionAspergillosis is a common cause of nasal infection in the dog,
affecting between 12% and 34% of dogs evaluated for chronic
sinonasal disease.1 It can cause a profuse mucopurulent to hem-
orrhagic nasal discharge, sneezing, reverse sneezing, ulceration of
the external nostrils, facial pain or discomfort, destruction and
necrosis of the nasal mucosa and underlying turbinate bones,
and frontal sinus osteomyelitis.1–3 Effective, noninvasive, safe, and
inexpensive treatment of dogs diagnosed with nasal aspergillosis is
challenging. Oral administration of antifungal agents such as
thiabendazole, ketoconazole, itraconazole, and fluconazole, al-
though noninvasive, requires prolonged administration due to
poor to moderate efficacy.4–8 In addition to the high cost of these
drugs, side effects such as hepatotoxicosis, anorexia, and vomiting
are commonly reported.7 Clinical cure is reported in approxi-
mately half of the patients treated with thiabendazole and keto-
conazole, and in as many as 70% of patients treated with
itraconazole or fluconazole.4
A topical 1 hr infusion with clotrimazole is considered an
effective noninvasive treatment that carries a 65% success rate after
one treatment and an 86–87% success rate with one or more
applications.9,10 More recently, endoscope-assisted debridement
followed by endoscope-assisted infusions with 1% or 2% enilco-
nazole were evaluated. The overall success rate of treatment of
dogs in either group (9 of 19 [47%] cured after one infusion, 6 of
19 [32%] after two infusions, and 2 of 19 [11%] after three
infusions of 1% enilconazole [total 89%]; 6 of 7 [85.7%] cured
after one infusion; the remaining dog cured after a second in-
fusion of 2% enilconazole) was similar to that previously reported
for noninvasive topical infusions.3 Another recent study evaluated
the efficacy of a 5 min flush of 1% clotrimazole delivered via
frontal sinus trephination followed by instillation of a 1% clo-
trimazole cream. Twelve of the 14 dogs (86%) responded well to
treatment and either had no clinical signs after treatment or had
signs consistent with mild rhinitis during a minimum follow up
of 6 mo. Only one dog required multiple treatments.11 This
treatment protocol, although offering comparable success rates
and shorter anesthesia than intranasal infusions of either clo-
trimazole or enilconazole delivered via catheters, is more invasive
and carries additional expense. For dogs that remain refractory to
From the Wilmington Animal Hospital, Wilmington, DE (S.E.); and
College of Veterinary Medicine, University of Minnesota, St. Paul,
MN (R.H.).
Correspondence: [email protected] (S.E.)
CT computed tomography
e110 JAAHA | 47:6 Nov/Dec 2011 ª 2011 by American Animal Hospital Association
any treatment, rhinostomy and topical povidine-iodine dressings or
rhinotomy combined with surgical debridement and topical ad-
ministration of 2% enilconazole may be indicated.4,12,13
Homeopathy is a system of medicine developed by the
German physician Samuel Hahnemann (1755–1843). It is based
on the principle of “let like cure like.” Substances, when tested,
can cause a set of symptoms in healthy individuals that are used to
cure those symptoms (signs in animals) when experienced by sick
individuals. The tests are known as “provings” and are conducted
using dilutions of the original substance.14
One of the first substances tested by Hahnemann was
a preparation of gold, aurum metallicum, in 1818 (six grains
triturated in 100 grains of milk sugar for 1 hr, then 100 grains of
this powder [1 grain of gold] or 200 grains of this powder [2 grains
of gold] dissolved in water [amount not specified] and given orally
to the human provers). This testing, along with his subsequent
prescribing of aurum metallicum to sick individuals (one part of
gold triturated to 100 parts of milk sugar, then one part of this to
100 additional parts of milk sugar, final dilution 1/10,000, given
orally, amount not specified), led him to discover the curative use
of aurum metallicum for painful, ulcerated nasal cavities and
nostrils, nasal congestion, greenish yellow nasal discharge, and
destruction of the palatal and nasal bones.15
The purpose of this report is to describe a case of nasal as-
pergillosis in a dog in which oral administration of homeopathic
aurummetallicum resulted in resolution of signs and disappearance
of the aspergillosis organisms after two noninvasive clotrimazole
infusions had been unsuccessful. This is the first reported case of
clinical resolution of nasal aspergillosis after treatment with aurum
metallicum inwhich follow-up studies were performed to document
the physical changes and clearance of the aspergillosis organisms.
Case ReportA 6 yr old, 33 kg, male, neutered Weimaraner was presented to the
University of Minnesota Veterinary Medical Center (VMC) for
evaluation of a 6–8 mo history of left-sided nasal discharge,
sneezing, and a 3 yr history of episodes of reverse sneezing. The
nasal discharge initially was clear to mucoid, but became purulent
with occasional mild epistaxis approximately 3 mo before pre-
sentation. The clinical signs were unresponsive to treatment with
oral diphenhydramine and clindamycin. During the 4 mo period
before presentation to the University of Minnesota VMC, the dog
became progressively more lethargic, and 1–2 mo before pre-
sentation, he developed a “snapping at flies” behavior accompanied
by continuous licking and crusting of the dorsal nasal planum.
Physical examination on day 1 showed a small amount of
crusting on the dorsal nasal planum, erosion and depigmentation
of the nasal planum, lack of airflow through the left nostril, and
blood-tinged serous nasal discharge on the left side that changed to
a mucopurulent discharge after a bout of sneezing. The left
submandibular lymph node was enlarged. Temperature, pulse, and
respiration were normal (38.88C, 120 beats/min, and 20 breaths/
min, respectively), as was a neurologic examination. A complete
blood count and serum biochemical profile were submitted. The
only significant laboratory abnormalities were hypoproteinemia
(5.2 g/dL; reference range 5.7–7.5 g/dL) and hypoalbuminemia
(2.3 g/dL; reference range 2.7–3.7 g/dL).
On day 2, nasal computed tomography (CT) and rhinoscopy
were performed. Extensive turbinate destruction was identified by
CTa within the rostral and midnasal passages on the left side.
Multifocal, patchy areas of fluid and thickened soft tissue material
were present, predominantly on the left side, but with some similar
appearing material on the right side. There was no evidence of
frontal sinus or maxillary bone destruction. Mild bone thickening
of the lateral ventral aspect of the left frontal sinus was present. The
cribriform plate was intact. Mild left-sided retropharyngeal and
submandibular lymphadenopathy were present. No other abnor-
malities were seen. The diagnostic interpretation was chronic de-
structive left-sided rhinitis and sinusitis with mild right-sided rhinitis
and secondary lymphadenopathy. A fungal disease was suspected;
differentials included aspergillosis and other fungal agents (Figure 1).
FIGURE 1 Nasal computed tomographic (CT) scan on day 2,
before clotrimazole infusion. Increase in soft tissue and fluid density
material as well as loss of normal turbinate architecture are present.
Homeopathic Treatment in Nasal Aspergillosis
JAAHA.ORG e111
Rhinoscopy, using both a 2.7 mm Stortz rigid telescopeb for
proximal visualization and an Olympus Exera II flexible video-
endoscopec for the retroflexed views of the nasopharynx, showed
a thick ropey discharge in the left nasal passage, loss of nasal
turbinates, hyperemia, and edema. Fungal plaques were visible in
the left nasal passages and nasopharyngeal meatus (Figure 2). The
right nasal passage was erythematous and edematous with no
turbinate destruction. Nasal biopsies were obtained with a 2.5 mm
flexible cup forcep biopsy instrumentd passed adjacent to the rigid
telescope. Cytology of the nasal discharge showed a moderate to
marked mixed inflammation (neutrophils, small lymphocytes,
plasma cells) and the presence of fungal organisms 5–8 mm in
diameter; these were basophilic and forming septate hyphae. His-
topathology showed severe fibrinosuppurative rhinitis with marked
infiltrates of neutrophils and debris, large areas of necrosis, and
extensive amounts of fungal organisms characterized by branching
hyphae. A fungal culture yielded growth of Aspergillus spp.
A 1 hr, 1% clotrimazolee infusion was performed according to
standard technique immediately after the CT scan and rhinos-
copy.9 Before the clotrimazole infusion, both nasal passages were
flushed antegrade and retrograde with salinef. Aggressive de-
bridement of visible fungal plaques was not performed, as this was
not known to be essential for treatment success at the time of this
rhinoscopy.4 The dog was discharged later the same day. Five days
later, due to the persistence of the nasal discharge and concern for
secondary bacterial infection, amoxicillin trihydrate/clavulanate
potassiumg was prescribed (11.4 mg/kg PO q 12 hr for 14 days).
On day 38 after the initial examination, the owner reported
recurrence of sneezing and left-sided nasal discharge, which had
ceased entirely for 3 wk immediately after the clotrimazole infusion.
Amoxicillin trihydrate/clavulanate potassium was again prescribed
for 14 days; however, the discharge continued and worsened. On
day 50 after the initial examination, the dog experienced a severe
episode of epistaxis. On day 71 after the initial examination, the dog
presented again to the University of Minnesota VMC with persistent
sneezing, nasal discharge, epistaxis, and facial pain. On the physical
examination performed on day 71 after initial presentation, the dog
was afebrile (38.88C) and had a left-sided serous nasal discharge,
depigmentation of his nasal planum, and crusting on the dorsal
nasal planum. The owner declined a second rhinoscopy before
a second 1% clotrimazole infusion was administered due to fi-
nancial constraints. Clotrimazole was again infused into each nasal
passage as previously performed on day 2. The dog was discharged
with amoxicillin trihydrate/clavulanate potassium (11.4 mg/kg PO q
12 hr for 14 days). One week later, the owner reported a left-sided
thick, yellow, ropey discharge and another episode of epistaxis. The
dog also appeared to be experiencing facial pain.
The dog was re-evaluated on day 115 (44 days after the second
treatment) by SE. A profuse yellow–brown odorous left-sided nasal
discharge was present, which persisted throughout the time after
the second clotrimazole infusion. In addition, the ulceration and
crusting of his nasal planum had progressed (Figure 3). The dog
continued to receive amoxicillin trihydrate/clavulanate potassium
since day 98. The primary care veterinarian gave two refills for 2 wk
FIGURE 2 Nasopharynx on day 2. Retroflexed view with white
plaques obstructing the left choanal area.
FIGURE3 Day 119. Severe ulceration, erythema, and crusting of
the nose of the dog before the aurum metallicum administration and
after two clotrimazole infusions.
e112 JAAHA | 47:6 Nov/Dec 2011
each (total of 6 wk). The dog exhibited pain when chewing and was
acting cold on his walks, wanting to turn around to go home. On
day 119, the homeopathic remedy aurum metallicum 30ch was
prescribed (5 pellets [size #38] dissolved in 15 mL of water PO
once, and then again one time 12 hr later). Improvement was noted
by the owner in the first week. Over the next 3 wk, the epistaxis
episodes ceased entirely, the nasal discharge gradually resolved, and
the dog’s disposition, appetite, and energy returned to normal.
Seven weeks after the homeopathic remedy administration,
the dog presented for a follow-up CT scan and rhinoscopy at the
University of Minnesota VMC.White blood cell count, hematocrit,
platelet estimate, red blood cell and white blood cell morphology,
total plasma protein, and serum biochemical profile were within
normal limits. The previously reported hypoalbuminemia and
hypoproteinemia had resolved (albumin, 2.7 g/dL and total protein,
6.6 g/dL). The CT scan showed that the previously noted turbinate
thickening on the left nasal passage was no longer present. A few
atrophied turbinates were present in the rostral nasal passages, but
the majority of the turbinates in the left nasal passage were com-
pletely absent (Figure 4). In the caudal nasal passages, the ventral
ethmoid turbinates remained, whereas the dorsal turbinates were
absent. The surrounding bone was thickened, and edematous soft
tissue was present at the periphery. The retropharyngeal lymph
nodes appeared normal in size, and the left submandibular lymph
node was only mildly enlarged with respect to the right. These
findings indicated that progressive destruction of the left nasal
turbinates occurred between the first and second CT scans. The
adjacent bone and soft tissue thickening suggested the presence of
residual disease. Rhinoscopy, with a 2.7 mm rigid telescope, verified
the lack of normal turbinate architecture. Minimal hyperemia or
discharge was visible within the left or right nasal passages, and no
fungal plaques were visualized. Mucosal biopsies were taken from
multiple sites in the left and right nasal passages. Histopathology
did not reveal fungal organisms, and mild residual lympho-
plasmacytic rhinitis was present.
Three to 4 mo later, the owners observed a crusty rough
appearance to the dorsal aspect of the dog’s nasal planum, and
a greenish, brownish, yellowish nasal discharge in the morning
that progressed from an occasional drip to a more persistent clear
drainage during the day. They also observed a slight recurrence of
reverse sneezing and the “biting at flies” behavior, both of which
had resolved after the homeopathic treatment. The owners were
instructed to repeat the aurum metallicum as previously pre-
scribed. Within a week of beginning administration of the aurum
metallicum, all of the dog’s abnormal clinical signs resolved,
according to the owner. At follow up on day 965 after initial
presentation, the dog remained asymptomatic, with only an oc-
casional reverse sneeze (Figure 5).
FIGURE 4 Nasal CT scan on day 164, 45 days postaurum
metallicum. Significant loss of nasal turbinates is evident as well as
mild thickening of residual nasal mucosa.
FIGURE 5 Dog’s nose 7 mo after the initial aurum metallicum
therapy. Some permanent remodeling of the left nasal planum is
present.
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JAAHA.ORG e113
DiscussionNasal aspergillosis is a common cause of nasal infection in the dog,
accounting for up to 34% of dogs with chronic nasal disease.1,16,17
Young to middle-aged dolichocephalic and mesaticephalic dogs
are most commonly affected, similar to the dog described in this
report.1 The fungal agent most commonly associated with the
disease is Aspergillus fumigatus, although A niger, A flavus, A
nidulans, and Penicillium sp. are occasionally involved.
Diagnosis of nasal aspergillosis is based on various combina-
tions of diagnostic tests, including diagnostic imaging, rhinoscopy,
sinuscopy, histologic examination, cytology, fungal culture, and
serology.18
In the dog described in this case report, a fungal plaque was
visualized via rhinoscopy and cultured positive for Aspergillus spp.
Fungal elements compatible with Aspergillus spp. were also seen
on cytology and further confirmed from biopsies obtained via
rhinoscopy. CT imaging also revealed changes compatible with
nasal aspergillosis.19–21
Initial treatment consisted of two infusions of topical clo-
trimazole without aggressive debridement. At the time this pro-
cedure was performed in this dog, debridement was not part of the
standard protocol at the University of Minnesota VMC. It is possible
that one reason for this dog’s treatment failure was the lack of
removal of as many fungal plaques as possible during the rhinos-
copy, which was performed only at the time of the first infusion.
A favorable response to conventional therapy is usually in-
dicated by resolution of nasal discharge by 2 wk after therapy.9
Rapid resolution of nasal pain, sanguinous discharge or epistaxis,
and ulcerated nares should occur.1 In some dogs, a mild muco-
purulent, crusty discharge may persist at one or both nostrils,
presumably as a result of the damaged nasal architecture.1 The
dog in this report had a short-lived response after the first clo-
trimazole infusion, but by 5 wk postinfusion, clinical signs re-
curred. The dog showed no response to the second infusion.
Repeat treatment is indicated if the nasal discharge persists by
2 wk after therapy.1,9 An additional clotrimazole infusion was
not performed as the owners elected to pursue homeopathic
treatment.
Homeopathic remedies are prescribed based on the concept of
“let like cure like.” A substance is given to healthy human provers,
who then record their mental, emotional, and physical symptoms
that arise as a result of the remedy’s effects. The symptoms are
collated and recorded in materia medicas and repertories. Symp-
toms and diseases that have been cured by remedies are also
recorded in these texts. These symptoms are then used as indi-
cations for the remedy to be administered when a sick patient
presents with these symptoms (or signs in the case of an animal).
In selecting the appropriate remedy, emphasis is given to signs
that are strong in the case (bone destruction, erosion of the nasal
planum, yellow malodorous nasal discharge) as well as signs that
differentiate one patient from another. Of special importance are
“modalities,” which include anything that makes a patient better
or worse, such as hot/cold weather, hot/cold compresses, time of
day, and seasons of the year.
In this case, the dog’s symptoms resolved after administration
of aurum metallicum, a homeopathic preparation derived from
gold. The dog’s signs of bone necrosis, including head pain, ulcer-
ated nostrils, yellow and malodorous nasal discharge, and aggra-
vation from being cold, corresponded with the signs documented
for aurum metallicum indications in the homeopathic provings and
materia medicas.15,22,23 In this case report, the dog was given a
preparation diluted 1:100, 30 times.
Homeopathic treatment is not fully dependent upon de-
lineation of an etiological agent. The characteristic symptoms
produced by the patient, regardless of the etiological agent, are used
for determining the remedy. However, insofar as certain etiologic
agents are known to produce fixed clinical signs in patients,
knowing that Aspergillus spp. were present in this dog could be
useful in determining the curative remedy. The results of the CT
scans and rhinoscopy, in describing the extent of the pathology in
this dog, were helpful in selecting the curative remedy.
After oral administration of the homeopathic remedy aurum
metallicum, the dog in this report experienced a dramatic clinical
improvement and disappearance of the Aspergillosis organisms.
Homeopathic treatment of nasal aspergillosis has been reported
once previously. 24 The dog in that report had a well-documented
case of nasal aspergillosis and showed an immediate curative re-
sponse to homeopathic therapy using the same remedy as in this
case. Although clinical signs appeared to resolve permanently in
that dog, the report did not include any follow-up studies.24 In the
case described here, follow-up studies, performed 7 wk after the
homeopathic remedy was given and all clinical signs of nasal dis-
charge resolved, showed that turbinate destruction on the left side
had progressed between the first CT, rhinoscopy, and clotrimazole
infusion and the second CT and rhinoscopy. Although the CT ev-
idence supported that the disease continued to progress sometime
between the first and second CT examinations, because the patient
had persistent signs consistent with nasal aspergillosis after a sec-
ond clotrimazole infusion and only showed resolution of disease
activity after the homeopathic remedy, the authors believed most of
the anatomic changes visualized on the second CTreflected damage
that occurred before the homeopathic remedy. The negative fungal
culture and histopathology obtained after the homeopathic remedy
supported that the disease was in complete remission at that time.
e114 JAAHA | 47:6 Nov/Dec 2011
The dog in this case had a mild relapse of signs 5 mo after the
homeopathic treatment. Given the brief and much milder pre-
sentation at that time, no diagnostics were done to verify whether this
was a recurrence of nasal aspergillosis. After the second treatment with
aurum metallicum, the signs promptly and permanently resolved.
The selection of a homeopathic medicine for a specific patient
is based on the patient’s unique characteristic manifestation of the
illness versus the etiological agent. However, as the clinical pre-
sentation of nasal aspergillosis in the dog remains relatively con-
stant, a narrow selection of homeopathic remedies might be useful.
Further pilot studies of the effects of aurum metallicum on nasal
aspergillosis, similar to a recently conducted study that used indi-
vidualized homeopathy to treat pruritus associated with atopic
dermatitis in dogs, are indicated.25 The results of such a study would
help determine the most useful homeopathic remedies for treat-
ment of nasal aspergillosis. Further studies, ideally using double-
blinded, placebo-controlled clinical trials, could then be conducted.
This case report was observational in nature but, in light of the
previously reported case, suggested that further study of the use of
aurum metallicum in cases of canine nasal aspergillosis should be
conducted.
This case report was supported in part by a grant from the Amer-
ican Holistic Veterinary Medical Association.
FOOTNOTESa GE HiSpeed CT/e spiral single-slice scanner; GE Healthcare,
Waukesha, WIb 2.7 mm Storz rigid telescope; Karl Storz Veterinary Endoscopy,
Goleta, CAc Olympus Exera II flexible videoendoscope; Olympus America Inc.,
Center Valley, PAd Flexible cup forcep biopsy instrument; Olympus America Inc.,
Center Valley, PAe Lotrimin; Schering Corporation, Kenilworth, NJf Saline; Baxter Corporation, Deerfield, ILg Clavamox; Pfizer Animal Health, Exton, PAh Boiron, Newtown Square, PA
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