Pediatric Case Reports
Epidural blockade for alternative
management of priapism: A case
report of child with T-cell acute
lymphoblastic leukemia
Ahmet Gokce, Deniz Gul, Mehmet Fatih Orhan, Mustafa B€ uy€ ukavci, Gurkan Demir, and
Serbulent Gokhan Beyaz
Priapism is a clinical condition that rarely presents with leukemia in childhood. Management of priapism treatment can
become more complex and difficult when accompanied by acute leukemia. We presented a 16 years old child with t-cell
acute lymphoblastic leukemia (ALL) who developed priapism. Due to the failure of conservative methods and intracaver-
nosal drainage, we performed epidural blockade which has limited data reported with successful results in the literature
before shunt surgery. UROLOGY 00: 1-3, 2021. © 2021 Elsevier Inc.
P
riapism is a pathological condition representing a
true disorder of penile erection that persists for
more than 4 hours and is beyond, or is unrelated
to, sexual interest or stimulation and remains despite
orgasm.
1
Basically, 3 main types of priapism are used in
classification and ischemic priapism accounts for 95% of
all cases.
2
Compartment syndrome in ischemic priapism
requires urgent medical intervention and irreversible con-
sequences such as corporal fibrosis and erectile dysfunc-
tion may occur if not treated quickly.
3,4
In terms of pathophysiology (Table 1), ischaemic pria-
pism has been identified as idiopathic in most cases.
2
Ischemic priapism is relatively more common (0.4%-
35%) after intracavernous injection of papaverine, phen-
tolamine and/or prostaglandin E1, but has also been asso-
ciated with sickle cell anemia (SCA), hematologic
dyscrasias, and neoplastic syndromes.
2,5,6
Leukemia is an important but relatively less common
cause of priapism in childhood. Most cases of leukemia
-associated priapism are chronic myeloid leukemia.
7
In
the literature, acute lymphoblastic leukemia (ALL) lead-
ing to priapism is very rare. In this report, we presented a
case of a 16 years old child who diagnosed as a T-cell ALL
and developed priapism and our alternative management
in priapism treatment.
CASE PRESENTATION
A sixteen-years-old, 66-kg male patient was admitted to
the emergency service with sudden blurred vision and
widespread rash on the body. Retinal bleeding was
detected in the fundoscopic examination. Laboratory
evaluation revealed 271 £ 10
9
/L of white blood cell
(WBC) and 97% of blast cell on peripheral blood smear.
T-cell ALL was diagnosed by flow cytometric analysis
(CD5: 93%, CD7: 55%, CD34: 43.6%, cCD3: 28.6%).
No blast was observed in cerebrospinal fluid. Brain MRI
and testicular ultrasound were normal. Prednisolone was
started in accordance with the ALL IC BFM 2009 proto-
col.
On the 3 day of the treatment, priapism developed with
penile pain and rigidity. Although leukemia is thought to
be the most likely cause of priapism, hemoglobin electro-
phoresis was performed to exclude SCA, which is the
most common disease in priapism etiology. Conservative
treatment as ice-pack, exercise, ejaculation and cold bath
were recommended at first-line immediately. As a result of
these conservative methods failed and priapism persisted,
twelve hours later, intracavernous drainage was planned
under sedation in the operating room. Lateral (3/9
o’clock) mid-shaft corporal needle access was performed,
avoiding the urethra or dorsal neurovascular bundle with
19G butterfly needle. In the first blood gas sample results,
pH:7.22, pCO
2
:63 mmHg and pO
2
:25 mmHg were deter-
mined and was consistent with ischemic priapism. After
the aspiration and irrigation, it couldn't achieve detumes-
cence, so intracavernosal epinephrine injection (2 mL of
1/100000 epinephrine solution with five times over a 20-
Disclosure: The authors declare that they have no known competing financial
interests or personal relationships that could have appeared to influence the work
reported in this paper.
From the Department of Urology, Sakarya University, Faculty of Medicine, Sakarya,
Turkey; the Department of Pediatric Hematology&Oncology, Sakarya University, Fac-
ulty of Medicine, Sakarya, Turkey; the Department of Anesthesiology and Reanimation,
Sakarya University, Faculty of Medicine, Sakarya, Turkey; and the Department of
Anesthesiology and Reanimation, Istinye University, Faculty of Medicine, Istanbul,
Turkey
Address correspondence to: Ahmet Gokce, M.D., Department of Urology, Sakarya
University School of Medicine, Sakarya, Turkey E-mails: aagokce@yahoo.com;
gokce@sakarya.edu.tr
Submitted: March 31, 2021, accepted (with revisions): June 17, 2021
1 https://doi.org/10.1016/j.urology.2021.06.017
0090-4295
© 2021 Elsevier Inc.
All rights reserved.
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