PubMed:23528907 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":110},"obj":"Sentence"},{"id":"TextSentencer_T2","span":{"begin":111,"end":251},"obj":"Sentence"},{"id":"TextSentencer_T3","span":{"begin":252,"end":438},"obj":"Sentence"},{"id":"TextSentencer_T4","span":{"begin":439,"end":577},"obj":"Sentence"},{"id":"TextSentencer_T5","span":{"begin":578,"end":728},"obj":"Sentence"},{"id":"TextSentencer_T6","span":{"begin":729,"end":906},"obj":"Sentence"},{"id":"TextSentencer_T7","span":{"begin":907,"end":1050},"obj":"Sentence"},{"id":"TextSentencer_T8","span":{"begin":1051,"end":1110},"obj":"Sentence"},{"id":"TextSentencer_T9","span":{"begin":1111,"end":1260},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":110},"obj":"Sentence"},{"id":"T2","span":{"begin":111,"end":251},"obj":"Sentence"},{"id":"T3","span":{"begin":252,"end":438},"obj":"Sentence"},{"id":"T4","span":{"begin":439,"end":577},"obj":"Sentence"},{"id":"T5","span":{"begin":578,"end":728},"obj":"Sentence"},{"id":"T6","span":{"begin":729,"end":906},"obj":"Sentence"},{"id":"T7","span":{"begin":907,"end":1050},"obj":"Sentence"},{"id":"T8","span":{"begin":1051,"end":1110},"obj":"Sentence"},{"id":"T9","span":{"begin":1111,"end":1260},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"A rare adolescent case of female pseudohermaphroditism with adrenocortical carcinoma and synchronous teratoma.\nA patient with female pseudohermaphroditism is chromosomally and gonadally a female individual but has male or ambiguous external genitalia. In this paper, we report a 12-year-old Chinese girl who was diagnosed with female pseudohermaphroditism characterized by clitoridauxe, hirsutism, acne, hypertension, and karyotype 46 XX. Computed tomography scan revealed a huge left abdominal mass with distant metastases to bilateral lungs and a concomitant pelvic teratoma. Because the left abdominal mass was unresectable, the patient underwent a biopsy of the abdominal mass and a radical resection of the pelvic teratoma. Histopathology confirmed that the left abdominal mass was an adrenocortical carcinoma (ACC) and the pelvic teratoma was a mature cystic teratoma originating from the left ovary. After surgery, the patient received a transcatheter arterial chemoembolization of ACC, combined with 2 g mitotane daily for systemic treatment. It was a pity that she died 8 months later after diagnosis. So far, as we know, the simultaneous occurrence of pseudohermaphroditism, ACC, and ovarian teratomas has not been reported in the literatures before."}

{"project":"Allie","denotations":[{"id":"SS1_23528907_5_0","span":{"begin":790,"end":814},"obj":"expanded"},{"id":"SS2_23528907_5_0","span":{"begin":816,"end":819},"obj":"abbr"}],"relations":[{"id":"AE1_23528907_5_0","pred":"abbreviatedTo","subj":"SS1_23528907_5_0","obj":"SS2_23528907_5_0"}],"text":"A rare adolescent case of female pseudohermaphroditism with adrenocortical carcinoma and synchronous teratoma.\nA patient with female pseudohermaphroditism is chromosomally and gonadally a female individual but has male or ambiguous external genitalia. In this paper, we report a 12-year-old Chinese girl who was diagnosed with female pseudohermaphroditism characterized by clitoridauxe, hirsutism, acne, hypertension, and karyotype 46 XX. Computed tomography scan revealed a huge left abdominal mass with distant metastases to bilateral lungs and a concomitant pelvic teratoma. Because the left abdominal mass was unresectable, the patient underwent a biopsy of the abdominal mass and a radical resection of the pelvic teratoma. Histopathology confirmed that the left abdominal mass was an adrenocortical carcinoma (ACC) and the pelvic teratoma was a mature cystic teratoma originating from the left ovary. After surgery, the patient received a transcatheter arterial chemoembolization of ACC, combined with 2 g mitotane daily for systemic treatment. It was a pity that she died 8 months later after diagnosis. So far, as we know, the simultaneous occurrence of pseudohermaphroditism, ACC, and ovarian teratomas has not been reported in the literatures before."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":126,"end":154},"obj":"HP_0010458"},{"id":"T2","span":{"begin":222,"end":250},"obj":"HP_0000062"},{"id":"T3","span":{"begin":327,"end":355},"obj":"HP_0010458"},{"id":"T4","span":{"begin":387,"end":396},"obj":"HP_0001007"},{"id":"T5","span":{"begin":398,"end":402},"obj":"HP_0001061"},{"id":"T6","span":{"begin":404,"end":416},"obj":"HP_0000822"},{"id":"T7","span":{"begin":568,"end":576},"obj":"HP_0009792"},{"id":"T8","span":{"begin":719,"end":727},"obj":"HP_0009792"},{"id":"T9","span":{"begin":790,"end":814},"obj":"HP_0006744"},{"id":"T10","span":{"begin":836,"end":844},"obj":"HP_0009792"},{"id":"T11","span":{"begin":865,"end":873},"obj":"HP_0009792"},{"id":"T12","span":{"begin":1194,"end":1211},"obj":"HP_0012226"},{"id":"T13","span":{"begin":1202,"end":1211},"obj":"HP_0009792"}],"text":"A rare adolescent case of female pseudohermaphroditism with adrenocortical carcinoma and synchronous teratoma.\nA patient with female pseudohermaphroditism is chromosomally and gonadally a female individual but has male or ambiguous external genitalia. In this paper, we report a 12-year-old Chinese girl who was diagnosed with female pseudohermaphroditism characterized by clitoridauxe, hirsutism, acne, hypertension, and karyotype 46 XX. Computed tomography scan revealed a huge left abdominal mass with distant metastases to bilateral lungs and a concomitant pelvic teratoma. Because the left abdominal mass was unresectable, the patient underwent a biopsy of the abdominal mass and a radical resection of the pelvic teratoma. Histopathology confirmed that the left abdominal mass was an adrenocortical carcinoma (ACC) and the pelvic teratoma was a mature cystic teratoma originating from the left ovary. After surgery, the patient received a transcatheter arterial chemoembolization of ACC, combined with 2 g mitotane daily for systemic treatment. It was a pity that she died 8 months later after diagnosis. So far, as we know, the simultaneous occurrence of pseudohermaphroditism, ACC, and ovarian teratomas has not been reported in the literatures before."}

{"project":"UBERON-AE","denotations":[{"id":"PD-UBERON-AE-B_T1","span":{"begin":176,"end":185},"obj":"http://purl.obolibrary.org/obo/UBERON_0000991"},{"id":"PD-UBERON-AE-B_T2","span":{"begin":232,"end":250},"obj":"http://purl.obolibrary.org/obo/UBERON_0004176"},{"id":"PD-UBERON-AE-B_T3","span":{"begin":537,"end":542},"obj":"http://purl.obolibrary.org/obo/UBERON_0002048"},{"id":"PD-UBERON-AE-B_T4","span":{"begin":895,"end":905},"obj":"http://purl.obolibrary.org/obo/UBERON_0002119"},{"id":"PD-UBERON-AE-B_T5","span":{"begin":959,"end":967},"obj":"http://purl.obolibrary.org/obo/UBERON_0001637"}],"text":"A rare adolescent case of female pseudohermaphroditism with adrenocortical carcinoma and synchronous teratoma.\nA patient with female pseudohermaphroditism is chromosomally and gonadally a female individual but has male or ambiguous external genitalia. In this paper, we report a 12-year-old Chinese girl who was diagnosed with female pseudohermaphroditism characterized by clitoridauxe, hirsutism, acne, hypertension, and karyotype 46 XX. Computed tomography scan revealed a huge left abdominal mass with distant metastases to bilateral lungs and a concomitant pelvic teratoma. Because the left abdominal mass was unresectable, the patient underwent a biopsy of the abdominal mass and a radical resection of the pelvic teratoma. Histopathology confirmed that the left abdominal mass was an adrenocortical carcinoma (ACC) and the pelvic teratoma was a mature cystic teratoma originating from the left ovary. After surgery, the patient received a transcatheter arterial chemoembolization of ACC, combined with 2 g mitotane daily for systemic treatment. It was a pity that she died 8 months later after diagnosis. So far, as we know, the simultaneous occurrence of pseudohermaphroditism, ACC, and ovarian teratomas has not been reported in the literatures before."}

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{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":60,"end":84},"obj":"ORDO:1501"},{"id":"AB1","span":{"begin":790,"end":814},"obj":"ORDO:1501"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"A rare adolescent case of female pseudohermaphroditism with adrenocortical carcinoma and synchronous teratoma.\nA patient with female pseudohermaphroditism is chromosomally and gonadally a female individual but has male or ambiguous external genitalia. In this paper, we report a 12-year-old Chinese girl who was diagnosed with female pseudohermaphroditism characterized by clitoridauxe, hirsutism, acne, hypertension, and karyotype 46 XX. Computed tomography scan revealed a huge left abdominal mass with distant metastases to bilateral lungs and a concomitant pelvic teratoma. Because the left abdominal mass was unresectable, the patient underwent a biopsy of the abdominal mass and a radical resection of the pelvic teratoma. Histopathology confirmed that the left abdominal mass was an adrenocortical carcinoma (ACC) and the pelvic teratoma was a mature cystic teratoma originating from the left ovary. After surgery, the patient received a transcatheter arterial chemoembolization of ACC, combined with 2 g mitotane daily for systemic treatment. It was a pity that she died 8 months later after diagnosis. So far, as we know, the simultaneous occurrence of pseudohermaphroditism, ACC, and ovarian teratomas has not been reported in the literatures before."}

{"project":"performance-test","denotations":[{"id":"PD-UBERON-AE-B_T1","span":{"begin":176,"end":185},"obj":"http://purl.obolibrary.org/obo/UBERON_0000991"},{"id":"PD-UBERON-AE-B_T2","span":{"begin":537,"end":542},"obj":"http://purl.obolibrary.org/obo/UBERON_0002048"},{"id":"PD-UBERON-AE-B_T3","span":{"begin":232,"end":250},"obj":"http://purl.obolibrary.org/obo/UBERON_0004176"},{"id":"PD-UBERON-AE-B_T4","span":{"begin":895,"end":905},"obj":"http://purl.obolibrary.org/obo/UBERON_0002119"},{"id":"PD-UBERON-AE-B_T5","span":{"begin":959,"end":967},"obj":"http://purl.obolibrary.org/obo/UBERON_0001637"}],"text":"A rare adolescent case of female pseudohermaphroditism with adrenocortical carcinoma and synchronous teratoma.\nA patient with female pseudohermaphroditism is chromosomally and gonadally a female individual but has male or ambiguous external genitalia. In this paper, we report a 12-year-old Chinese girl who was diagnosed with female pseudohermaphroditism characterized by clitoridauxe, hirsutism, acne, hypertension, and karyotype 46 XX. Computed tomography scan revealed a huge left abdominal mass with distant metastases to bilateral lungs and a concomitant pelvic teratoma. Because the left abdominal mass was unresectable, the patient underwent a biopsy of the abdominal mass and a radical resection of the pelvic teratoma. Histopathology confirmed that the left abdominal mass was an adrenocortical carcinoma (ACC) and the pelvic teratoma was a mature cystic teratoma originating from the left ovary. After surgery, the patient received a transcatheter arterial chemoembolization of ACC, combined with 2 g mitotane daily for systemic treatment. It was a pity that she died 8 months later after diagnosis. So far, as we know, the simultaneous occurrence of pseudohermaphroditism, ACC, and ovarian teratomas has not been reported in the literatures before."}