Splenic haemangioma and Kasabach-Merritt Syndrome as differential diagnosis for abdominal mass in a newborn: case report

نویسنده

  • CHV Mariño
چکیده

Pós-graduando da Seção de Cirurgia Pediátrica. Instituto Nacional de Câncer, Hospital do Câncer I, Rio de Janeiro, RJ Brasil. Médico Cirurgião Pediátrico da Seção de Cirurgia Pediátrica. Instituto Nacional de Câncer, Hospital do Câncer I, Rio de Janeiro, RJ Brasil. Médico Patologista da Seção de Anatomopatologia. Instituto Nacional de Câncer, Hospital do Câncer I, Rio de Janeiro, RJ Brasil. Médico Cirurgião Pediátrico, Chefe da Seção de Cirurgia Pediátrica. Instituto Nacional de Câncer, Hospital do Câncer I, Rio de Janeiro, RJ Brasil. Enviar correspondência para A.R.G. E-mail: [email protected] Recebido em maio de 2001 Abstract We report a rare case of splenic haemangioma in the form of an abdominal mass in a 20-dayold female newborn with coagulopathy and thrombocytopenia. She was operated on, and the mass was found to be a tumor of the inferior pole of the spleen. She remains well after six months of follow-up. The diagnostic and treatment options are reviewed and discussed. The authors reviewed the literature about splenic haemangioma in newborns, noticing that it is the third reported case associating splenic haemangioma and Kasabach-Merritt Syndrome. Splenic haemangioma is a rare differential diagnosis to abdominal masses in newborns. Haemangioma is the most frequent benign neoplasm of the spleen. Anemia, thrombocytopenia and coagulopathy are often found in patients with large cavernous haemangioma associated with Kasabach-Merritt syndrome (KMS). The development of splenic haemangiomas in that syndrome is extremely rare in newborns.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A new successful combination therapy with atenolol and prednisolone for Kasabach-Merritt syndrome

Kasabach-merritt syndrome is a rare life-threatening syndrome associated with vascular tumors such as tufted angioma and kaposiform hemangioendothelioma. For this syndrome, there exist a few treatment modalities with variable results. For many years, corticosteroids have been employed in the first-line therapy. Nowadays, on the other hand, β blockers such as propranolol have been used owing to ...

متن کامل

Successful treatment of kasabach-merritt syndrome with vincristine and surgery: a case report and review of literature

INTRODUCTION Haemangiomas are vascular lesions resulting from abnormal proliferation of blood vessels. They are the most common pediatric neoplasm. Kasabach-Merritt syndrome is a rare type of vascular lesion with peculiar characteristics. The diagnosis is based upon three basic findings; enlarging haemangioma, thrombocytopenia and consumption coagulopathy. CASE PRESENTATION A 5 month old boy ...

متن کامل

Coexistence of cystic intra-abdominal lymphangiomas and diffuse venous haemangiomas in adult life.

Diffuse haemangioma and intra-abdominal lymphangioma are rare in adults. In this case report, we present a 33-year-old female with coexisting multiple cutaneous and visceral cavernous haemangiomas and two huge intra-abdominal lymphangiomas of 25 and 35 cm in diameter. The organs involved were the liver, pericardium, renal hilus and bladder. She died due to disseminated intravascular coagulation...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2002