1.A life‑threatening benign vascular lesion of the uterus, cavernous hemangioma: A case report
Maria Lalaine Aviles Miranda ; Eleyneth Ilagan Valencia
Philippine Journal of Obstetrics and Gynecology 2023;47(5):283-290
The objective of this clinical report is to present the first local case of rare cavernous uterine
hemangioma. This is a case of a 28‑year‑old G2P1 (1001) during her first trimester of pregnancy
who was admitted to our institution for the second time due to profuse vaginal bleeding and
severe anemia. The transvaginal scan revealed an embryonic demise of 8 weeks age of gestation
noted at the endocervical canal. There is a posterofundal heterogeneous mass measuring
6.3 cm × 5.7 cm × 5.0 cm (volume: 94.2 ml) with multiple cystic spaces, which on Doppler studies
showed abundant vascularity suggestive of uterine hemangioma. Antifibrinolytics were administered.
The patient underwent emergency hysterectomy with bilateral salpingectomy due to profuse
vaginal bleeding with histopathology result of cavernous hemangioma of the uterus. Cavernous
uterine hemangioma is a rare vascular lesion that poses a great challenge in the diagnosis and
management. There were limited published articles regarding cavernous hemangioma of the uterus.
There were conservative treatment options such as uterine artery embolization, the use of hormonal
oral contraception, intralesional glucocorticoid therapy, the use of interferon‑α, laser therapy, and
surgical excision. Hysterectomy is the definitive treatment for intractable bleeding. It is recommended
to establish an international registry for this rare case. The experts in different specialties such as
obstetrician‑gynecologists, interventional radiologists, and vascular surgeons, can also formulate
an algorithm for its diagnosis and treatment.
Case Reports
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Hemangioma
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Vascular Malformations
2.“Blocked broken heart syndrome”: an unusual case of a complete atrioventricular block complicating a Takotsubo cardiomyopathy
A. BRIOSA ; J. SANTOS ; A. C. GOMES ; O. SIMÕES ; R. MIRANDA ; S. ALMEIDA ; L. BRANDÃO ; H. PEREIRA
International Journal of Arrhythmia 2022;23(3):18-
Background:
Complete heart block is considered a unique and rare complication of Takotsubo cardiomyopathy, an otherwise self-resolving disease. When this occurs, there is a double clinical dilemma: first to find out which triggered the other and second, to decide whether or not to implant a permanent pacemaker.Case presentation: We present a case of a 77 years-old female patient, with previous medical history of arterial hypertension, diabetes mellitus, dyslipidemia and bifascicular block known since 2013. She came to the emergency department after recurrent syncopal episodes. At admission a complete heart block was diagnosed, and it was implanted a single chamber temporary pacemaker. The patient remained in disproportional acute decompensated heart failure despite pacemaker implantation. She denied chest pain although referring an episode of self-limiting chest pain 2 days before, after an argument with the family. Blood analysis showed an important rise in NTproBNP and troponin levels. Transthoracic echocardiogram showed a dilated left ventricle with akinesia of apical and mid segments, hyperkinesia of basal segments and severely depressed left ventricle ejection fraction. Coronary angiography showed no significant lesions and the diagnosis of Takotsubo cardiomyopathy was suspected. During the following days, she recovered her own intrinsic rhythm. Electrocardiogram evolved with deep T-wave inversion and prolonged QT interval and transthoracic echocardiogram showed resolution of the previous alterations. Despite complete reversion of rhythm alteration, it was decided to implant a permanent pacemaker.
Conclusions
We describe a rare, life-threatening and often underdiagnosed complication of the stress cardiomyopathy. Furthermore, we performed a literature revision of this rare complication and discussed the therapeutic challenge encountered in such patients.
3.3-Dimensional fasciectomy: A highly efficacious common ground approach to Dupuytren's surgery.
Benjamin H MIRANDA ; Charlotte ELLIOTT ; Christopher C KEARSEY ; David N HAUGHTON ; Mark R WEBB ; Ian HARVEY ; Fahmy S FAHMY
Archives of Plastic Surgery 2018;45(6):557-563
BACKGROUND: Numerous Dupuytren’s fasciectomy techniques have been described, each associated with unique surgical challenges, complications and recurrence rates. We describe a common ground surgical approach to Dupuytren’s disease; 3-dimensional fasciectomy (3DF). 3DF aims to address the potential contributors to the high recurrence rate of Dupuytren’s disease and unite current limited fasciectomy practice that varies considerably between surgeons. METHODS: We describe the 3DF principles; raising thin skin flaps (addressing dermal involvement), excising diseased palmar fascia with a 3−5 mm clearance margin (treating highly locally recurrent conditions) and excising the vertical septae of Legueu and Juvara (providing deep clearance, hence addressing all potentially involved pathological tissue). The surgical outcomes between traditional limited fasciectomy (LF) and 3DF are compared. RESULTS: From the 786 operations included (n=585), postoperative recurrence rates were significantly lower for the 3DF group (2/145, 1.4%) than the LF group (72/641, 11.2%) (P=0.001), and the time to recurrence was significantly longer (5.0±0 years vs. 4.0±0.2 years; P < 0.0001). With recurrence excluded, there were no differences between the postoperative complication rates for 3DF (5/145, 3.5%) and LF (41/641, 6.4%) (P=0.4). CONCLUSIONS: Our results suggest that 3DF leads to lower recurrence rates and a longer disease-free period for patients, without increasing complications. 3DF provides a safe, efficacious, common ground surgical approach in the treatment of Dupuytren’s flexion deformity.
Congenital Abnormalities
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Dupuytren Contracture
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Fascia
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Hand
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Humans
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Postoperative Complications
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Recurrence
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Skin
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Surgeons
4.Stent versus Balloon Dilation for the Treatment of Dominant Strictures in Primary Sclerosing Cholangitis: A Systematic Review and Meta-Analysis
Marina Tucci Gammaro Baldavira FERREIRA ; Igor Braga RIBEIRO ; Diogo Turiani Hourneaux DE MOURA ; Thomas R. MCCARTY ; Alberto Machado DA PONTE NETO ; Galileu Ferreira Ayala FARIAS ; Antônio Afonso DE MIRANDA NETO ; Pedro Victor Aniz Gomes DE OLIVEIRA ; Wanderley Marques BERNARDO ; Eduardo Guimarães Hourneaux DE MOURA
Clinical Endoscopy 2021;54(6):833-842
Background/Aims:
The endoscopic management of primary sclerosing cholangitis (PSC)-associated dominant strictures remains challenging. This systematic review and meta-analysis aimed to compare balloon dilation and stent placement in the treatment of dominant strictures among PSC patients.
Methods:
Literature searches on MEDLINE, EMBASE, Cochrane CENTRAL and Lilacs/Bireme were performed for studies published until December 2020. Measured outcomes included clinical efficacy, stricture recurrence, cumulative recurrencefree rate, transplant rate, 5-year survival rate, and adverse events (i.e., pancreatitis, cholangitis, bleeding, perforation and death).
Results:
A total of 5 studies (n=467) were included. Based on pooled analyses, there were no differences in clinical efficacy (risk difference [RD], -0.13; 95% confidence interval [CI], -0.58 to 0.33; I2=93%) or transplant rates (RD, -0.09; 95% CI, -0.19 to 0.01; I2=0%); however, the risk of occurrence of adverse events was lower with balloon dilatation than with stent placement (RD,-0.34; 95% CI, -0.45 to -0.23; I2=61%). Among the types of adverse events reported, only the rates of cholangitis/bacteremia were significantly lower in balloon dilation patients (RD, -0.19; 95% CI, -0.25 to -0.13; I2=51%).
Conclusions
Compared to balloon dilation, stent placement for dominant strictures in PSC appeared to have higher complication rates without significant differences in efficacy.