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Antenatal sonographic diagnosis of fetal sacrococcygeal teratoma with hydrops--(a case report).

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A rare case of sacrococcygeal teratoma (SCT) associated with hydrops diagnosed on prenatal ultrasound and subsequently confirmed on parturition is presented.

Mediastinal teratoma as a rare cause of hydrops fetalis and death: report of 3 cases.

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BACKGROUND Congenital mediastinal teratomas are rare and may present with nonimmune hydrops. The lesion may be misinterpreted on ultrasound. METHODS A 21-year-old woman, gravida 2, para 0111, was evaluated at 19 4/7 weeks of gestation for suspected fetal death. An ultrasonogram confirmed the death

Antenatal diagnosis of large sacro-coccygeal teratoma with foetal cardiomegaly and hydrops.

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We report the case of a young primigravida who presented with a 20 weeks pregnancy with a previous diagnosis of uterine fibroid. However, ultrasound evaluation revealed the presence of a large sacro-coccygeal teratoma in the foetus which was heterogeneous with cystic areas and calcific foci, and

Delayed surgery in pericardial teratoma with neonatal hydrops.

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Timing of neonatal surgery in cases of pericardial teratoma with hydrops is not standardised. We report two cases of hydropic premature newborns with pericardial teratoma in which surgery was delayed until respiratory and haemodynamic stabilisation. Mature teratoma was removed on day 3. The newborns

Intrapericardial teratoma causing nonimmune hydrops fetalis and pericardial tamponade: a case report.

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A case of fetal anasarca secondary to an intrapericardial teratoma is reported. The clinical, echocardiographic, and histologic features are described, along with a review of intrapericardial lesions.

Massive ovarian edema and contralateral mature cystic teratoma: asymptomatic presentation in a premenarchal female.

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BACKGROUND Massive ovarian edema is a rare entity, which in most cases occurs in adult females presenting with abdominal pain. We present an unusual case associated with contralateral teratoma in a premenarchal female. METHODS A 13-year-old asymptomatic female presenting with an abdominopelvic mass

Non-immunological hydrops fetalis and intrapericardial teratoma: case report and review.

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A large intrapericardial teratoma was found at necropsy in a 38-week stillborn fetus, in which prenatal diagnosis of hydrops fetalis and an echogenic cardiac mass had been made. Clinical and pathological data are reported. In utero intrapericardial teratomata lead to different outcomes depending on

Intrapericardial teratoma with hydrops leading to in utero demise.

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We report a case of intrapericardial teratoma following in utero demise at 29 weeks with nonimmune hydrops. The diagnosis was strongly suggested by ultrasound findings and confirmed by fetopathology. The mechanism whereby intrapericardial teratomas may lead to hydrops and death is massive

Hydrops fetalis caused by intrapericardial teratoma.

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A case of hydrops fetalis caused by an intrapericardial teratoma is presented. The importance of establishing the etiology of a hydropic state in utero is described, as active neonatal care seems to improve the outcome for these babies, although the mortality is still very high.

Massive ovarian edema with contralateral mature cystic teratoma--a case report of an uncommon combination.

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A case with massive ovarian edema (MOE) of left ovary--a rare pseudotumour and mature cystic teratoma of right ovary is described in a young unmarried girl of 16 years. The etiopathological concepts, morphological changes and differential diagnosis are described. Knowledge about the entity and its

Hydrops fetalis and neonatal abdominal compartment syndrome continuum from immature gastric teratoma: a case report.

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Hydrops fetalis as well as abdominal compartment syndrome (ACS) are conditions that are associated with high mortality rates. A rare case of immature gastric teratoma causing fetal hydrops and subsequent ACS is presented. The related pathophysiologic mechanisms are discussed, and the

A case of mediastinal teratoma as a cause of nonimmune hydrops fetalis, and literature review.

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This article reviews the current literature of mediastinal tumors as the cause of nonimmune hydrops fetalis (NIHF), the outcomes of reported cases, and a general overview of NIHF including diagnosis, workup, and a management algorithm, with particular attention made to intrathoracic lesions and

Antenatal diagnosis of sacrococcygeal teratoma with hydrops fetalis; a case report.

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Fetal sacrococcygeal teratoma (SCT) with hydrops fetalis is known to have a poor prognosis. We report a case of SCT with hydrops fetalis which was diagnosed antenatally at 30 weeks gestation. After delivery by cesarean section, the tumor was removed and the infant is alive one year after surgery

The newborn with hydrops and sacrococcygeal teratoma.

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The combination of fetal hydrops and sacrococcygeal teratoma (SCT), is considered to be lethal. We report two such babies who survived. Case 1 exhibited oliguric acute renal failure (ARF) immediately after birth, and severe respiratory insufficiency despite maximal ventilatory support and

Successful management of a large fetal mediastinal teratoma complicated by hydrops fetalis.

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This report describes a case of fetal mediastinal teratoma complicated by hydrops fetalis managed successfully by aspiration of the tumor cyst fluid. Fetal mediastinal teratomas are rare tumors that cause hydrops fetalis or fetal demise in the prenatal period and respiratory distress in the neonatal

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