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1.
BMJ Case Rep ; 17(3)2024 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-38429060

RESUMEN

Laparoscopy for intra-abdominal exploration and tissue sampling is useful in advanced ovarian cancers, in which it is presumed to be difficult to achieve complete tumour reduction in the initial surgery. This is a report of a case of suspected advanced ovarian cancer in a patient, who underwent laparoscopic screening and was later pathologically diagnosed with tuberculous peritonitis. A woman in her 50s visited her local doctor with constipation. Since imaging showed massive ascites she was referred for further evaluation. We initially suspected advanced ovarian cancer due to the presence of massive ascites and multiple peritoneal nodules. However, histopathological examination indicated that the nodules were tubercles, and the patient was subsequently diagnosed with tuberculous peritonitis. It is important to be aware that tuberculosis peritonitis can be misdiagnosed or mistaken for advanced ovarian cancer. Preoperative diagnosis of tuberculous peritonitis is often difficult. Tuberculous peritonitis should be considered if intraoperative findings show diffuse nodular disseminated lesions.


Asunto(s)
Neoplasias de los Genitales Masculinos , Laparoscopía , Neoplasias Ováricas , Peritonitis Tuberculosa , Femenino , Humanos , Ascitis , Peritonitis Tuberculosa/diagnóstico , Peritoneo , Carcinoma Epitelial de Ovario , Neoplasias Ováricas/complicaciones , Neoplasias Ováricas/diagnóstico , Neoplasias Ováricas/cirugía
2.
J Obstet Gynaecol Res ; 43(4): 775-778, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28418207

RESUMEN

Pyoderma gangrenosum (PG) is a rare ulcerative skin disease that usually starts as a pustular lesion and rapidly progresses to a painful ulcer with undermined violaceous borders. The occurrence of PG during pregnancy is uncommon. We describe a case of a pregnant patient with PG who was diagnosed as having ulcerative colitis after delivery. Obstetricians need to understand the pathogenesis of PG and its associated conditions because it is important to make a proper diagnosis and provide targeted therapy.


Asunto(s)
Complicaciones del Embarazo/diagnóstico , Piodermia Gangrenosa/diagnóstico , Adulto , Femenino , Humanos , Embarazo , Complicaciones del Embarazo/patología , Complicaciones del Embarazo/fisiopatología , Piodermia Gangrenosa/patología , Piodermia Gangrenosa/fisiopatología
3.
Gynecol Oncol ; 145(2): 407-408, 2017 05.
Artículo en Inglés | MEDLINE | ID: mdl-28237617

RESUMEN

OBJECTIVE: High paraaortic lymph nodes superior to the renal vein are often involved by metastasis from advanced ovarian cancer, but are difficult to dissect. We developed a novel surgical technique for removing these nodes. METHODS: The ascending colon is displaced from the right paracolic gutter. A retroperitoneal incision is made cranially from the ileocecal region along Monk's white line (fusion fascia) dorsal to the ascending colon. Incising the fusion fascia toward the root of the right renal vein from inside Gerota's fascia allows separation of the right kidney and mobilization of the ascending colon, partly exposing the inferior vena cava. Then the inferior vena cava below the renal vein is exposed by dissecting the right ovarian vein. Next, Kocher's maneuver is performed [1,2]. After mobilizing the duodenum, the inferior vena cava can be fully exposed below the left hepatic lobe. Then the peritoneum is incised from near the aortic bifurcation along the inferior mesenteric vein toward the ligament of Treitz, allowing complete mobilization of the small intestine and right hemicolon. Placing these viscera extra-abdominally in isolation bags provides excellent visualization of the entire aorta from the superior mesenteric artery to common iliac artery. RESULTS: This method can completely remove the high paraaortic nodes, followed by the paraaortic nodes inferior to the renal vein, without complications. CONCLUSIONS: This surgical technique for dissection of the high paraaortic lymph nodes is convenient, safe, and easy to learn. It is considered to be advantageous for management of ovarian, primary peritoneal, or fallopian tube cancer.


Asunto(s)
Neoplasias de las Trompas Uterinas/cirugía , Escisión del Ganglio Linfático/métodos , Ganglios Linfáticos/cirugía , Neoplasias Ováricas/cirugía , Neoplasias Peritoneales/cirugía , Neoplasias de las Trompas Uterinas/patología , Femenino , Procedimientos Quirúrgicos Ginecológicos/métodos , Humanos , Ganglios Linfáticos/patología , Neoplasias Ováricas/patología , Neoplasias Peritoneales/patología
4.
Clin Pract ; 5(1): 722, 2015 Jan 28.
Artículo en Inglés | MEDLINE | ID: mdl-25918634

RESUMEN

Primary retroperitoneal mucinous cystic tumors with borderline malignancy are rarely encountered. To date, only 12 cases have been reported in the literature. In this report, we present an additional case. A 65-year-old nulliparous woman complained of abdominal fullness. Her medical history included a hysterectomy and a single salpingo-oophorectomy performed 25 years prior to the present event. Physical examination revealed a large cystic mass in the abdomen and pelvis. During laparotomy, a cystic tumor measuring 21×14 cm in size was observed in the left retroperitoneal space. The tumor was resected, and the final diagnosis was primary retroperitoneal mucinous cystic cancer with borderline malignancy.

5.
Clin Pract ; 4(1): 605, 2014 Mar 27.
Artículo en Inglés | MEDLINE | ID: mdl-24847429

RESUMEN

A 40-year old woman, gravida 4, para 4, presented with sudden lower abdominal pain and severe vaginal bleeding at 17 weeks of gestation. Clinical symptoms and ultrasonographic finding revealed placental abruption. The volume of bleeding was heavy and led to disseminated intravascular coagulation and hypovolemic shock. We performed blood transfusion and therapy to treat the critical condition. However, the mother's condition continued to worsen. Therefore, we performed a hysterotomy and aborted the pregnancy to save the mother. Since heavy bleeding caused by placental abruption leading to a life-threatening condition for a mother before the 20 weeks of gestation is very rare, the present case is an important case study.

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