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IMAGING DIAGNOSIS—A LUMINAL LAMINATED DEBRIS BALL

IN THE URINARY BLADDER OF A DOG

HAKYOUNG YOON, HANJIN KIM, UOOK JUNG , KIDONG EOM

A 5-year-old dog presented with pollakiuria and urinary incontinence. Abdominal radiographs revealed an
oval, multilayered structure with soft tissue opacity and gas lucency in the urinary bladder. Ultrasonography
showed an oval luminal structure with hyper- and hypoechoic layers and internal reverberation artifacts.
Following cystotomy, the hemisected plane showed a layered, pale whitish matrix with a gas layer around the
core. Histopathological examination showed no evidence of cells, bacteria, or fungi. The core and laminae
comprised fibrinous and mineral debris. A final diagnosis of a freely floating, gas-filled laminated debris ball
was made.  C 2016 American College of Veterinary Radiology.

Key words: canine, gas, laminated ball, radiography, ultrasonography, urinary bladder.

Signalment, History, and Clinical Findings

A 5-YEAR-OLD SPAYED FEMALE MINIATURE poodle dog


weighing 3.9 kg presented with depression, pollak-
iuria, and urinary incontinence. Physical examination re-
vealed 5%–7% dehydration. Abnormal laboratory find-
ings included elevated glucose (236 mg/dl; reference range,
74–143 mg/dl) and alkaline phosphatase (773 mg/dl; refer-
ence range, 23–212 mg/dl) levels. A complete blood count
revealed neutrophilia (19,000/µl; reference range, 4000–
12,600/µl) and an increased hematocrit (59%; reference in-
terval, 39%–56%). After radiography and ultrasonography
were performed, a urine sample was collected by cysto-
centesis. The specimen revealed proteinuria and glycosuria.
Abnormalities in urine cytology included a marked num-
ber of bacilli, neutrophils, and urinary bladder transitional
cells. Urine culture was performed, which identified Es-
cherichia coli and Streptococcus spp. exhibiting sensitivity
to enrofloxacin. FIG. 1. An abdominal radiograph shows a right lateral view of a 5-year-old
dog that presented with pollakiuria and urinary incontinence. One large air
bubble (asterisk) and a laminated ball (black arrow) with an outer radiolucent
Imaging, Diagnosis and Outcome area (white arrowhead), inner radiolucent area (white arrow), and radiopaque
layers can be observed.
Abdominal radiographs revealed a fluid-filled stomach
and blunted caudoventral hepatic margins protruding cau- in the urinary bladder (Fig. 1). A large gas bubble around
dal to the costal arch. Notably, an oval, multilayered struc- the ball was identified on a lateral view.
ture with soft tissue opacity and gas lucency was observed Abdominal ultrasonography revealed a fluid-filled stom-
ach and hyperechoic liver with a fine echotexture. In the
urinary bladder, a freely floating, oval structure with multi-
From the Department of Veterinary Medical Imaging, College of
Veterinary Medicine (Eom, Yoon); College of Veterinary Medicine ple hyperechoic and hypoechoic layers was seen (Fig. 2A).
and Veterinary Science Research Institute (Eom), Konkuk University, Multiple hyperechoic foci were present in this laminated
Seoul, 143-701, Korea, and Haedam Animal Hospital, Gwanmyeong-si, object. While some cast an acoustic shadow (Fig. 2B), oth-
Gyeonggi-do, Korea (Kim, Jung).
Address correspondence and reprint requests to Kidong Eom, at the ers created reverberation artifacts (Fig. 2A and B). Color
above address. E-mail: eomkd@konkuk.ac.kr
Received December 29, 2015; accepted for publication May 9, 2016.
doi: 10.1111/vru.12385 Vet Radiol Ultrasound, Vol. 00, No. 00, 2016, pp 1–4.

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FIG. 2. Ultrasonographic images (A and B) and gross appearance (C and D) of a laminated ball found in the urinary bladder of a 5-year-old dog. On
ultrasonography (A and B), a hyperechoic and hypoechoic multilayered (asterisk) laminated ball shows reverberation artifacts within the empty spaces (white
arrow) observed between some layers in gross examination (D). A thick, outer hypoechoic layer (arrowhead) surrounded by a thin, outer hyperechoic layer
can be observed on ultrasonography (B), which appears as a pale, whitish matrix on gross examination (D). The ball demonstrates a yellowish-white color and
smooth surface (C).

Doppler examination revealed no flow within the structure. but firmer than a marshmallow. The length, height, and
Gravity-dependent hyperechoic sediment and free gas with width were 17, 13, and 12.5 mm, respectively. The ball was
reverberation artifacts were also identified in the urinary hemisected in saline; air bubbles escaped during hemisec-
bladder. On the basis of laboratory, radiographic, ultra- tion. The hemisected surface showed a concentrically lam-
sonographic, and cytological examinations, tentative diag- inated structure, similar to a cut onion (Fig. 2D). Some of
noses of diabetes mellitus, urinary infection, and a luminal the radiolucent areas observed on the radiographs likely
mass in the urinary bladder were made. Differential diag- corresponded to the matrix, which was pale and whitish.
noses for the luminal mass included a hematoma, foreign Empty spaces were observed between some inner layers in
body, bacterial stone, fungal ball, and laminated fibrinous the ball.
ball. Considering that all of these could account for the The core and borders of each layer of the ball showed
clinical presentation, surgical removal was scheduled. positive staining with hematoxylin and eosin, periodic
Cystotomy was performed under general anesthesia. The acid–Schiff, and Masson’s trichrome; however, the thick
luminal structure was an oval ball with a yellowish-white outer matrix of the ball did not show definitive staining
color and smooth surface (Fig. 2C). It was soft to the touch, (Fig. 3A–C). Sporadic mineral infiltration was identified
VOL. 00, NO. 00 LAMINATED DEBRIS BALL IN A CANINE BLADDER 3

FIG. 3. Histopathological findings after hematoxylin and eosin staining (A, D, G), periodic acid–Schiff staining (B, E, H), and Masson’s trichrome staining
(C, F, I) of a laminated ball found in the urinary bladder of a 5-year-old dog. Microscopic views under 12.5× (A, B, C), 40× (D, E, F), and 400× (G, H, I)
magnifications show the general, core, and layer margin findings, respectively. Empty spaces can be observed between some layers (black arrow).

in each of the layer margins, which were stained with ously reported in dogs. Laminated fungal1 and fibrinous2–4
hematoxylin and eosin (Fig. 3D and G). However, collage- balls similar to the one found in the present case have been
nous tissue that would show a blue signal with Masson’s reported in humans. In vitro experiments have suggested
trichrome staining was not observed in any region (Fig. that laminated calcium phosphate stones may develop via
3C). No cells, bacteria, or fungal hyphae were observed. a polymer-induced, liquid-like precursor phase in the pres-
Therefore, the structure was diagnosed as a laminated de- ence of abundant organic molecules in urine,5 while lami-
bris ball composed of fibrin and debris without infectious nated fungal and fibrinous balls occur mainly in immuno-
agents, despite the identification of several bacteria in urine compromised patients such as those with diabetes mellitus
cytology. and neoplasia.2,6 Patients with fungal balls can show neg-
After surgery, the dog exhibited normal urination, and ative results for fungal infection in a routine urine culture,
she did not present any clinical symptom related to cys- while several fungal hyphae and spores can be identified
totomy for 7 months since the surgery, as confirmed by in histopathological examination.1,6,7 In a laminated fibri-
telephone interviews with the owner. nous ball, blood clots and tissue debris may function as a
nucleus for the formation of amorphous fibrin material.3
In the present case, diabetes mellitus was responsible for
Discussion an immunocompromised status. Although several bacilli
Unattached, freely floating, concentrically laminated were identified, no fungal hyphae or spores were observed
balls in the urinary bladder with gas and gas-like radi- in urine cytology. Furthermore, cultures of samples ob-
olucent regions are extremely rare and have not been previ- tained from within the laminated ball showed neither fungi
4 YOON ET AL. 2016

nor bacteria. Although the distinct etiology of the ball was cytology and culture, the presence of anaerobic bacteria
unclear, the authors consider that the underlying pathogen- could explain the free gas within the urinary bladder.
esis was similar to that of fibrinous and fungal balls that de- In conclusion, to the best of our knowledge, this is the
velop from the organization of necrotic tissue or fibrinous first report describing an unattached, freely floating lami-
or lithiasic debris.2,3,8 In the present case, bacteria were nated debris ball in a canine urinary bladder. A laminated
not observed in the histopathological examination. How- debris ball should be included as a differential diagnosis
ever, cell debris and fibrin associated with severe urinary in dogs with a round mass exhibiting multiple radiolucent
infection could have agglutinated, rolled, and sequentially and radiopaque layers on radiography and appearing as an
formed a laminated ball. Therefore, we considered this lam- unattached, freely floating, concentric multilayered ball on
inated debris ball to be different from previously reported ultrasonography in the urinary bladder. However, further
laminated fibrinous and fungal balls.2,6 All these balls can studies are required to determine the etiology and con-
grow progressively in size and obstruct the lower urinary stituents of this phenomenon.
tract; therefore, surgical removal is mandatory.1,8
Interestingly, trapped gas was identified between some LIST OF AUTHOR CONTRIBUTIONS
layers on radiography and ultrasonography and during Category 1
hemisection of the laminated ball. This indicated the pos-
sibility of the existence of gas-forming bacteria within the (a) Conception and Design
ball at some point in time. In the present case, the ball was Hakyoung Yoon, Kidong Eom
(b) Acquisition of Data
clearly visible on abdominal radiographs because of the ra- Hakyoung Yoon, Hanjin Kim, Uook Jung
diolucent regions. On the other hand, most fungal and fib- (c) Analysis and Interpretation of Data
rinous balls without gas exhibit soft tissue opacity, similar Hakyoung Yoon, Uook Jung, Hanjin Kim
to urine, and cannot be detected on routine radiographs.1,3
Category 2
Note that some portion of the radiolucent area was
hypoechoic on ultrasonography and did not stain with (a) Drafting the Article
hematoxylin and eosin, periodic acid–Schiff, or Masson’s Hakyoung Yoon
trichrome. Loosely organized, dehydrated debris, and de- (b) Revising Article for Intellectual Content
bris containing lipids and other radiolucent ingredients Hanjin Kim, Uook Jung, Hakyoung Yoon, Kidong Eom
may account for some of the radiolucent areas observed Category 3
on radiographs.9
Free luminal gas within the urinary bladder could be due (a) Final Approval of the Completed Article
to gas-forming bacteria. Before radiographic and ultra- Kidong Eom, Hakyoung Yoon, Hanjin Kim, Uook Jung
sonographic examinations, no procedure such as urinary ACKNOWLEDGMENT
catheterization, cystocentesis, or fine-needle aspiration of This study was supported by Veterinary Science Research Institute of
the laminated ball had been performed. From routine urine The Konkuk University.

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3. Carruthers NC. Vesical fibrin stone. Can Med Assoc J 1959;80: in the bladder. J Urol 1961;86:559–562.
284–286. 8. Praz V, Burruni R, Meid F, Wisard M, Jichlinski P, Tawadros T.
4. Marcus R, Brewer AC. Fibrinoma of the bladder. Br J Urol Fungus ball in the urinary tract: a rare entity. Can Urol Assoc J 2014;8:
1951;23:156–159. E118–E120.
5. Amos FF, Dai L, Kumar R, Khan SR, Gower LB. Mechanism of 9. McLeod BC, Charters JR, Straus AK, Kuo KN. Gas-
formation of concentrically laminated spherules: implication to Randall’s like radiolucencies in a popliteal cyst. Rheumatol Int 1983;3:
plaque and stone formation. Urol Res 2009;37:11–17. 143–144.

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