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Acquired Hemophilia A Diagnosed Based on Gross Hematuria: A Case Report and Literature Review.
Hata, Kenichi; Kato, Junichiro; Takahashi, Yusuke; Saito, Shun; Sakanaka, Keigo; Kimura, Takahiro.
Afiliação
  • Hata K; Department of Urology Atsugi City Hospital, 1-16-36, Mizuhiki, Atsugi City, Kanagawa-ken 243-8588, Japan.
  • Kato J; Department of Nephrology Atsugi City Hospital, 1-16-36, Mizuhiki, Atsugi City, Kanagawa-ken 243-8588, Japan.
  • Takahashi Y; Department of Urology Atsugi City Hospital, 1-16-36, Mizuhiki, Atsugi City, Kanagawa-ken 243-8588, Japan.
  • Saito S; Department of Urology Atsugi City Hospital, 1-16-36, Mizuhiki, Atsugi City, Kanagawa-ken 243-8588, Japan.
  • Sakanaka K; Department of Urology Atsugi City Hospital, 1-16-36, Mizuhiki, Atsugi City, Kanagawa-ken 243-8588, Japan.
  • Kimura T; Department of Urology Jikei University School of Medicine, 3-25-8, Nishishinbashi, Minatoku, Tokyo 105-8461, Japan.
Case Rep Urol ; 2024: 2760153, 2024.
Article em En | MEDLINE | ID: mdl-39161780
ABSTRACT
Acquired hemophilia A (AHA) is an acquired bleeding disorder caused by neutralizing antibodies (inhibitors) against Coagulation Factor VIII (FVIIIC), causing sudden hemorrhagic symptoms (i.e., subcutaneous bleeding, intramuscular bleeding, and hematuria). Herein, this study is aimed at presenting a case of AHA diagnosed based on hematuria and reviewing patients who were diagnosed with AHA due to hematuria. A 67-year-old woman was referred to Atsugi City Hospital with painless gross hematuria that began 4 weeks before presentation. Contrast-enhanced computed tomography (eCT) revealed an approximately 2 cm mass in the right renal pelvis, and the patient's activated partial thromboplastin time (APTT) was elevated (61.4 s). The day after the endoscopic biopsy, the patient was in shock due to a large retroperitoneal hematoma. Although her condition stabilized after intravenous radioembolization, she underwent emergency surgeries several times because of rebleeding within the next 3 weeks. At that time, APTT was more prolonged at 106.4 s, and the FVIIIC level was 2%. Mixing tests showed an upwardly convex curve after 2-h incubation, indicating the presence of an inhibitor. Factor VIII inhibitor titer was ≥5.1 Bethesda unit (BU)/mL. A combined product of Plasma-Derived Factors VIIa and X (pd-FVIIa/FX), as second-line hemostatic therapy, as well as cyclophosphamide (CYP), were administered after Recombinant Activated Factor VIIa (rFVIIa) had been ineffective. Following this, the Factor VIII inhibitor titer was undetectable, FVIIIC levels were restored, and APTT decreased to within the normal range. Gross hematuria was significantly alleviated. However, the patient died of cytomegalovirus and fungal infections due to prolonged immunosuppressive therapy. Although AHA diagnosed based on hematuria may have a better prognosis than others, there have been occasional cases with severe outcomes. APTT, detected upon initial hematological testing in patients with hematuria, may be a potential indicator of an existing AHA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Case Rep Urol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Case Rep Urol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Estados Unidos