Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report
Patient: Female, 70-year-old Final Diagnosis: Solitary fibrous tumor Symptoms: Hypoglycemia • urinary retention Medication: — Clinical Procedure: Surgical resection Specialty: Laboratory Diagnostics • Obstetrics and Gynecology • Pathology • Surgery
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| Veröffentlicht in: | The American journal of case reports 2022-10, Vol.23, p.e936806-e936806 |
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| container_title | The American journal of case reports |
| container_volume | 23 |
| creator | Deguchi, Yasunori Komuta, Wataru Watanabe, Tomokazu Saiga, Kazuho Kurahashi, Koki Otsuka, Kazuo Hirata, Koji Mizumoto, Masaki Kitaoka, Akihiro Zaima, Masazumi |
| description | Patient: Female, 70-year-old
Final Diagnosis: Solitary fibrous tumor
Symptoms: Hypoglycemia • urinary retention
Medication: —
Clinical Procedure: Surgical resection
Specialty: Laboratory Diagnostics • Obstetrics and Gynecology • Pathology • Surgery |
| doi_str_mv | 10.12659/AJCR.936806 |
| format | Article |
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Final Diagnosis: Solitary fibrous tumor
Symptoms: Hypoglycemia • urinary retention
Medication: —
Clinical Procedure: Surgical resection
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Final Diagnosis: Solitary fibrous tumor
Symptoms: Hypoglycemia • urinary retention
Medication: —
Clinical Procedure: Surgical resection
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Final Diagnosis: Solitary fibrous tumor
Symptoms: Hypoglycemia • urinary retention
Medication: —
Clinical Procedure: Surgical resection
Specialty: Laboratory Diagnostics • Obstetrics and Gynecology • Pathology • Surgery</abstract><pub>International Scientific Literature, Inc</pub><pmid>36227783</pmid><doi>10.12659/AJCR.936806</doi><oa>free_for_read</oa></addata></record> |
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| identifier | ISSN: 1941-5923 |
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| issn | 1941-5923 1941-5923 |
| language | eng |
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| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
| title | Successful Surgical Treatment of a Recurrent Pelvic Solitary Fibrous Tumor of Uterine Origin Accompanied by Doege-Potter Syndrome: A Case Report |
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