scholarly journals Sarcomatous tumor of the right ovary, removed by laparotomy in the gynecological department at the Mogilev obstetric institution

2020 ◽  
Vol 9 (7-8) ◽  
pp. 631-639
Author(s):  
S. Lipinsky

Unfortunately, we do not yet have accurate statistics of malignant neoplasms of the ovaries. Virkhov, for example, of the opinion that they are quite rare. In Schroeder's 600 cases of neoplasms of the ovaries, there are only 10 cases of malignant, consequently somewhat more than 1%. Wert in relation to ovarian cysts determines the frequency of dense neoplasms in 5%. Spencer Wells initially rose 1.72%, followed by even less 1.2%. Leopold), from a more distant time, there are only 8 cases of malignant neoplasms of the ovaries: 4 cases of Spencer Wlls, of which two were fatal, two cases of Spiegelberg, both were fatal, one case of Buren and one recovered a rural doctor whose patient died of a collapse shortly after the operation. Even if we assume that cases of malignant neoplasms of the ovaries are quite rare, then all the same, judging by the latest reports, it cannot be argued that this rarity would be in such a scale as the authors just cited for a longer time estimate it.

2021 ◽  
Vol 25 (4) ◽  
pp. 278-283
Author(s):  
D. A. Malysheva ◽  
A. A. Sukhotskaya ◽  
V. G. Bairov ◽  
I. M. Kagantsov ◽  
N. A. Kokhreidze ◽  
...  

Introduction. Neonatal ovarian cysts develop in case of hormonal imbalance in the mother-placenta-fetus system. Cystic transformation in the ovary may cause appendage torsion which leads to follicular necrosis and loss of ovarian reserve. Most often, torsion occurs in the utero, but in premature girls- due to the specific hormonal status - the risk of cyst growth and its torsion remains in the postnatal period. Currently, a unified approach to the surgical treatment of neonatal ovarian cysts is absent.Material and methods. In the department of pediatric surgery for malformations in the Perinatal Center of the Amazov National Medical Research Center, 34 girls with ovarian cysts were examined during 2012-2020; 9 of them (27%) were premature. In the presented observation, we faced an ovarian cyst in the fetus of 30 week gestation.Results. The cyst looked uncomplicated, but had the enormous size, so we discussed a possibility to perform an intrauterine puncture. However, due to severe hemolytic disease of the fetus and premature delivery, the intervention was not carried out. By the third week of life, torsion of the cystic-transformed ovary developed; necrosis and self-amputation of the right uterine appendage were revealed intraoperatively. By the age of three months, cystic transformation of the only ovary developed. Timely performed laparoscopic fenestration was organ-sparing. Further follow-up revealed preserved and normally growing single ovary what confirmed the right choice of surgical tactics.Conclusion. Dynamic ultrasound examination of the pelvic organs is indicated to all premature girls, at least once every two weeks (in case of revealed ovarian cyst - weekly). We consider it reasonable to make the laparoscopic fenestration of uncomplicated cysts that have size of 3 cm and more. Newborn girls with ovarian cysts should be under the joint control of pediatrician and pediatric gynecologist for developing an individual follow-up plan.


2021 ◽  
Vol 108 (Supplement_7) ◽  
Author(s):  
Charles Scott ◽  
Anthony Lambert

Abstract Introduction Females of reproductive age with a clinical diagnosis of appendicitis may undergo laparoscopy prior to appendicectomy. This paper advocates laparoscopy after appendicectomy only if the appendix is macroscopically normal in this patient group.  Method A cohort of patients under the care of a single general surgeon is reported. If the appendix was macroscopically normal a laparoscopic port was inserted through the right iliac fossa incision. This single port was used for laparoscopic assessment of the pelvic organs. Results Fourteen females of reproductive age underwent laparoscopy following a macroscopically normal open appendicectomy. No additional laparoscopic ports were required. A benign dermoid ovarian cyst was identified in a 14 year-old which was electively excised following further investigation by a gynaecologist. Two ruptured simple ovarian cysts were also identified. There were no complications reported in this patient group. Conclusions Laparoscopy following a macroscopically normal open appendicectomy allows assessment of the pelvic organs in females of reproductive age and reduces the number of ports required during surgery.  


2016 ◽  
Vol 6 (1) ◽  
pp. 70-74
Author(s):  
Shikha Satish Bhatt

ABSTRACT Osteosarcomas (OS) are malignant neoplasms of the bone that commonly affect the long bones with rare presentation in jaws. Osteosarcomas of jaws represent about 6 to 8% of all OS, with an incidence of approximately 1 in 1.5 million persons per year. Although the exact cause of OS is still unknown, defects in the retinoblastoma (RB) and p53 genes play an important role in the process. It is characterized histologically by anaplastic stroma with direct osteoid production. Here, we report a case of OS in a 30-year-old female, who came with a massive bony swelling in the right mandibular region. How to cite this article Bhatt SS, Patel S, Pathak J, Swain N. Osteosarcoma of Mandible. J Contemp Dent 2016;6(1):70-74.


2021 ◽  
Vol 9 (4) ◽  
pp. 859-862
Author(s):  
Fahd Idarrha ◽  
Youness Aznague ◽  
Yassine Fathlkhir ◽  
Brahim Demnati ◽  
Abass Guedi Omar ◽  
...  

Background:Myopericytoma (MPC) is term that describe a rare group of perivascular tumours of soft tissue and show a range of histological growth patterns. Only a few cases describing MPC have been reported. Aims: To document and investigate the clinical and histopathological characteristics and differential diagnosis of myopericytoma. Patients/methods: The present study reports a unique case of myopericytomas found in the 2nd and 3rd inter-toe spaces of a 54-year-old patient. Results: a 54 year old female patient, presents in our department for a painless mass on the dorsal surface of the right forefoot of progressive installation over 2 years.The mass was firm, non pulsatile and mobile, with no sign of inflammation, evolving in a context of conservation of the general state. The X-ray of the right forefoot did not reveal any notable bone abnormality. An MRI was subsequently performed, which objectified an infiltrating tumor mass of probable sarcomatous origin. The mass was excised surgically, and a pathological and immunohistochemical examination was performed afterward, the diagnosis of myopericytoma was confirmed. No recurrence was found in the follow-up of 12 months. Conclusions: MPC is a rare and mostly benign tumor that presents as spindle cells in a concentric perivascular growth model with an immunohistochemical staining positive for smooth muscle actin. Local recurrences and rarely metastases may occur in atypical and malignant neoplasms.


Mastology ◽  
2020 ◽  
Vol 30 (Suppl 1) ◽  
Author(s):  
Marina Fontes Medeiros ◽  
Soraya de Paula Paim ◽  
Rachel Saraiva Teatini Selim de Sales ◽  
Thássia Mariz de Melo ◽  
Janaina Cotta Rodrigues Ferreira

Introduction: Sarcomas are a heterogeneous group of malignant neoplasms and represent less than 1% of neoplasms among adults; 80% of these cases originate in soft tissues. The liposarcoma corresponds to 20% of the subtypes of sarcoma in adults. Objectives: To present a rare case of liposarcoma of the breast. Methods: We studied the case of A.N.R, a 54-year old male patient, from Belo Horizonte, Minas Gerais, presenting a progressive growth nodule in the right breast. Mammography and breast ultrasound suggested lipoma. Core-needle biopsy of the nodule in the right breast was performed, and the anatomopathological was compatible with lipoma. Case report: Due to the progressive growth, the patient was submitted to nodule resection, with safety margins. Anatomopathological and immunohistochemical of the surgical piece were compatible with well-differentiated liposarcoma. The patient was followed-up by the oncologist and had a staging computed thoracic and abdominal tomography without changes, thus not indicative of adjuvant treatment. Discussion: Liposarcoma presents as a painless mass, of progressive growth, being more common in extremities and the retroperitoneum. When the well-differentiated morphological subgroup is located in the extremities and the torso, its excision is curative, and its metastatic potential is null in comparison to other locations; however, it is not recommended to underestimate the risk of local recurrence. Conclusion: even though the prevalence of benign lesions in soft tissues is higher than malignant lesions, it is important to consider a differential diagnosis of malignancy when the behavior and presentation of the tumor are atypical (deep location to the muscle fascia, larger than 5 centimeters, progressive growth), therefore leading to better surgical and therapeutic planning and to a more accurate treatment for the patient.


Author(s):  
S. Siew ◽  
B. Newton

Testicular germinal tumors are the most common malignant neoplasms in young men. We had the opportunity to examine a case of embryonal carcinoma of the testis by means of transmission (TEM), scanning (SEM) electron microscopy and energy dispersive x-ray analysis. The propositus was a man of 21 years of age, who complained of left testicular discomfort, which radiated to the left anterior superior spine in the inguinal area. On examination, the right testis was normal. There was slight enlargement of the left testis with a definite nodularity, medially, where there was a very firm area. The epididymis was normal on palpation. Surgical resection was performed with removal of the left testis and dissection of the retroperitoneal lymph nodes. The testis measured 5.2x3.4x3 cm. On section, it had a lobulated appearance. There was gross evidence of extension into the rete testis but the tunica albuginea was not penetrated and the epididymis was normal.


2020 ◽  
Vol 5 (7) ◽  

Ovarian torsion is a condition that can occur in a normal ovary, but it is more likely to happen when the presence of a cyst or other tissues (tumor) in the ovary can displace it. The extra weight or mass on the ovary can cause it to start to twist and rotate around its supporting ligaments. Ovarian torsion can cause severe pain, more frequently on the right-hand side. However, in some cases, the clinical course is prolonged, as the torsion can be intermittent. Early diagnosis and surgery are essential to protect ovarian and tubal function and prevent severe morbidity ending with annessiectomy. The ovarian cyst is an insidious risk factor for ovarian torsion and can cause sudden lower abdominal pain and loss of ovarian function with possible legal implications and malpractice. A timely diagnosis of ovarian cyst is of paramount importance to prevent necrosis and preserve ovarian viability. To avoid such a dangerous complication, it is essential the preventive management of the cyst. A cyst becomes a problem when it does not go away or gets bigger. The treatment of ovarian cysts depends on several factors but the size of the cyst and its appearance need to be monitored.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. A690-A690
Author(s):  
Marianne Jacob ◽  
Dix Poppas ◽  
Oksana Lekarev

Abstract Background: Precocious puberty in girls is defined as onset of secondary sexual characteristics, such as breast development, before 8 years of age. To differentiate between central and peripheral precocious puberty, laboratory and imaging evaluation is helpful. When gonadotropins are low but estradiol is elevated, results may suggest a primary ovarian source of estrogen production. Small ovarian cysts are not uncommon, are benign and self-resolve. However, large ovarian cysts are rare, let alone ones requiring surgical removal. Clinical Case: A 6 year 7 month old girl presented with several days of breast tenderness and palpable bilateral breast tissue noted by her mother. There was no history of vaginal bleeding. There were no reported exposures to estrogen-containing products. Her mother reached menarche at age 14 years. The patient was born full term and was otherwise healthy. On exam, her height was at the 90-95th %ile (mid-parental height at the 95th %ile) and her growth velocity was 10.9 cm/yr. She had Tanner 2 breasts (1 cm breast bud on the left and 1.5 cm on the right), Tanner 1 pubic hair and no axillary hair, body odor, acne or café-au-lait macules. A bone age was read as 6 years at a chronological age of 6 years 7 months. A laboratory evaluation revealed an estradiol of 1,029 pg/mL (<15 pg/mL), LH <0.02 mIU/mL, FSH <0.09 mIU/mL, 17-hydroxyprogesterone (17-OHP) 410 ng/dL (<91 ng/dL), AFP 2.3 ng/mL (<6.1 ng/mL), beta-hCG <2 mIU/mL, TSH 2.41 mIU/L (0.5-3.2 mIU/L), and free T4 0.9 ng/dL (0.9-1.4 ng/dL). Pelvic ultrasound revealed a large unilocular cystic structure measuring 6.5 x 4.1 x 6.1 cm in the left adnexal region with no left ovary visualized. The right ovary appeared prepubertal. The uterus was prepubertal in appearance with endometrial thickness of 2 mm. Abdominal ultrasound showed no evidence of a suprarenal mass. A laparoscopic cyst resection was completed, given the risk of left ovarian torsion. Cytology was negative; pathology revealed a luteinized follicular cyst. Repeat labs in one month showed a prepubertal estradiol level of 6.7 pg/mL with LH 0.02 mIU/mL and FSH 0.38 mIU/mL. 17-OHP normalized to 29 ng/dL. Breast tissue had regressed. Conclusion: This case describes the rare finding of a large luteinized follicular ovarian cyst that required surgical removal in a 6-year-old girl in the setting of a significantly elevated estradiol level. Luteinized follicular cysts have been described in newborns, though rare. To our knowledge, this is the first described case of a luteinized follicular cyst in this patient’s age group. Laboratory and imaging evaluation should be considered in girls presenting with precocious puberty, despite the extent of thelarche, as the clinical examination does not always correlate with degree of estradiol elevation. This is especially important if clinical changes are acute and other features are consistent with puberty, such as rapid linear growth.


2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
W. S. L. De Silva ◽  
S. R. De Almeida ◽  
G. D. B. J. Karunarathne ◽  
A. A. S. Samarathunga ◽  
K. M. C. S. Gannoruwa ◽  
...  

Introduction. The genitourinary system is a recognized site for multiple primary malignant neoplasms even without syndromic anomalies. However, to the best of our knowledge, a case of upper tract urothelial carcinoma (UTUC) with contralateral renal cell carcinoma (RCC) is not reported in surgical literature so far. Case Presentation. A 52-year-old Sri Lankan male patient was found to have a right lower ureteric tumour and a left renal mass together upon investigating for painless visible hematuria. The right ureteric tumour measured 32 × 22   mm resulting in moderate hydronephrosis and cortical thinning of the right kidney, and the left renal mass measured 43 × 38   mm involving the lower pole. The biopsy of the right ureteric lesion revealed a high-grade transitional cell carcinoma with focal nested pattern and that of the left renal mass revealed a clear cell carcinoma. Right nephroureterectomy followed by a left partial nephrectomy was performed in six weeks’ interval. The histology of both the resected specimens confirmed the biopsy findings. Discussion. A high-risk upper tract urothelial carcinoma such as the right ureteric tumour of this patient required a nephroureterectomy which makes the management of the contralateral renal cell carcinoma more complex. An adequate functional renal remnant was ensured after offering oncologically sound surgical treatment for both the malignancies of this patient. Conclusion. A UTUC when associated with a contralateral RCC poses challenges in patient management. The preservation of renal excretory function has to be considered as an important determinant in addition to oncologically sound surgical resection when managing complex cases of genitourinary malignancies involving both sides of the upper urinary tract.


1938 ◽  
Vol 34 (2) ◽  
pp. 203-205
Author(s):  
N. Kh. Sitdykov

Malignant neoplasms of the kidney are uncommon. According to German statistics, there are less than 1% of malignant kidney tumors per 100,000 autopsies. Ravasini found only 22 cases of malignant neoplasms of the kidneys and adrenal glands at 10,034 autopsies. In Lenequin's statistics for 10 years, out of 796 cancers, only one case of kidney cancer is indicated. According to Davydovsky's statistics, out of 2765 cases of malignant neoplasms, only 31 cases are in the kidneys.


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