scholarly journals Pseudotumor Tuberculosis Of Liver: A Rare Entity

2015 ◽  
Vol 1 (1) ◽  
pp. 1-6
Author(s):  
Mehdi Soufi ◽  
Ghizlane Kharrasse ◽  
Khanoussi wafae ◽  
Zahi Ismaili ◽  
Tijani El haroudi ◽  
...  
Keyword(s):  
Abdominal Pain ◽  
Liver Biopsy ◽  
Rare Case ◽  
Histopathological Examination ◽  
Laboratory Data ◽  
Abdominal Imaging ◽  
Recurrent Fever ◽  
Rare Entity ◽  
Isolated Liver

We present a rare case of a 46-year-old man who presented with recurrent fever and abdominal pain without other symptoms. Laboratory data were no specific for diagnosis. Abdominal imaging revealed a pseudotumor liver. A diagnosis of isolated liver tuberculosis with abscess component was confirmed with US-guided liver biopsy and histopathological examination. The patient received antibacillous drugs with success.

scholarly journals Ovarian Hemangioma: a rare entity

2018 ◽  
Vol 7 (6) ◽  
pp. 2490
Author(s):  
Mona Dahal ◽  
Paricha Upadhyaya ◽  
Purbesh Adhikari ◽  
Diksha Karki ◽  
Niraj Regmi
Keyword(s):  
Abdominal Pain ◽  
Cavernous Hemangioma ◽  
Cystic Lesion ◽  
Radical Surgery ◽  
Histopathological Examination ◽  
Correct Diagnosis ◽  
Lower Abdominal Pain ◽  
Surgical Excision ◽  
Vascular Tumors ◽  
Rare Entity

Ovarian hemangiomas are uncommon benign vascular tumors of ovary. Most of them are asymptomatic and detected incidentally during surgery. Authors report a case of 41 years female, parity 2; with complain of lower abdominal pain for 6 months. Ultrasonography showed a cystic lesion at right adnexa with a heterogeneously echogenic component within and devoid of internal vascularity. Laparoscopic right adnexal cystectomy was done, which on histopathological examination demonstrated features of cavernous hemangioma replacing the ovarian parenchyma. As surgical excision is treatment of choice, correct diagnosis is essential to avoid unnecessary radical surgery and treatment.

scholarly journals A rare case of perineal endometriosis with anal sphincter involvement

2020 ◽  
Vol 9 (3) ◽  
pp. 1268
Author(s):  
Bhadana Priyanka ◽  
Abha Kiran ◽  
Veena Ganju Malla
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Preoperative Evaluation ◽  
Subsequent Development ◽  
Perineal Ultrasound ◽  
Rare Entity ◽  
Scar Endometriosis ◽  
Malignant Changes ◽  
Perineal Endometriosis

Perineal endometriosis is a rare entity which can be explained by direct implantation of endometriotic cells over the fresh episiotomy wound and subsequent development of scar endometriosis. Perineal scar endometriosis incidence is reported to be 0.3% to 1%. 28 years old, P1L1, presented with pain and swelling near episiotomy site which is associated with menstruation. Examination during menstruation revealed swelling was tender, erythematous and slightly increased in size. Clinical diagnosis of scar endometriosis was made after clinical examination. Mass excised and sent for histopathological examination. Although diagnosis essentially remains clinical, preoperative evaluation with perineal ultrasound and MRI was performed. Wide local excision remains treatment of choice and follow up for recurrence is recommended. Histopathological examination is obligatory to exclude rare possibility of malignant changes.

scholarly journals Placental Polyp : A Rare Case Report

2021 ◽  
Vol 20 (2) ◽  
pp. 85-88
Author(s):  
Most Sabina Yeasmin ◽  
Nishat Anjum Nourin ◽  
Tahera Begum ◽  
Farah Naz Mabud ◽  
Farjana Ahmed Surovi
Keyword(s):  
Case Report ◽  
Vaginal Bleeding ◽  
Rare Case ◽  
Histopathological Examination ◽  
Elevated Serum ◽  
Placental Tissue ◽  
Rare Entity ◽  
Definite Diagnosis ◽  
Rare Case Report ◽  
One Year

Placental polyp is the retained fragment of placental tissue which presents as a polypoidal or pedunculated mass within the uterus. It is a rare entity and has an incidence of less than 0.25 % of all pregnancies. There are also very few reported cases of the clinical placental polyp. Here,we report a case of 22-year-old P1 woman presenting with vaginal bleeding and something coming down into vagina.Her last pregnancy had occurred one year ago.Laboratory investigation revealed slightly elevated serum b-hCG. Ultrasonography revealed thick endometrium, broad cervix (5.2cm) and a hyperechoic mass within the cervix. Extraction of the placental polyp followed by endometrial curettage were done and tissue sent for histopathology. Definite diagnosis was made by histopathological examination and which was a placental polyp. Chatt Maa Shi Hosp Med Coll J; Vol.20 (2); July 2021; Page 85-88

scholarly journals A rare case of gastric fundus tuberculosis with nonspecific abdominal pain

2021 ◽  
Vol 49 (7) ◽  
pp. 030006052110331
Author(s):  
Feiyu Yan ◽  
Xianzhe Yu ◽  
Hongjun Lei ◽  
Yi Chen ◽  
Jiwei Wang ◽  
...  
Keyword(s):  
Abdominal Pain ◽  
Rare Case ◽  
Histopathological Examination ◽  
Submucosal Tumor ◽  
Treatment Delay ◽  
Gastric Fundus ◽  
Abdominal Symptoms ◽  
High Incidence ◽  
Upper Abdominal ◽  
Space Occupying Lesion

A 53-year-old patient who experienced recurring upper abdominal pain and discomfort for 4 years was admitted to our hospital. Gastroscopy was performed to identify the location of the pain and evaluate the characteristics of a mass in the abdomen. Endoscopic ultrasonography (EUS) and abdominal computed tomography (CT) revealed a space-occupying lesion in the gastric fundus, suggestive of a submucosal tumor and highly likely of stromal origin. Surgical resection of the lesion was performed for identification; however, postoperative histopathological examination of the lesion revealed gastric fundus tuberculosis (TB). Gastric TB is relatively rare; therefore, clinicians should be highly suspicious of patients with abdominal symptoms from regions with a high incidence of TB to prevent treatment delay caused by misdiagnosis.

scholarly journals An Unusual Presentation of Small Bowel Intussusception

2021 ◽  
pp. 9-11
Author(s):  
Yinglin Gao ◽  
Cheikh Talal El Imad ◽  
Hai Song Kim ◽  
Vivek Gumaste
Keyword(s):  
Abdominal Pain ◽  
Small Bowel ◽  
Rare Case ◽  
Recurrent Abdominal Pain ◽  
Nausea And Vomiting ◽  
Adult Intussusception ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Small Bowel Intussusception ◽  
Intestinal Obstructions

Adult small bowel intussusception is a very rare entity that accounts for 5% of all cases of intussusception and 1%–5% of intestinal obstructions. It is more common in children but can occur in adults. It is an important etiology to consider when a patient presents with recurrent abdominal pain. The diagnosis can be challenging as symptoms are nonspecific and include abdominal pain, nausea and vomiting. This paper presents a rare case of duodenal intussusception, followed by a review of the literature discussing the diagnosis and treatment of adult intussusception.

scholarly journals Mixed Mucinous and Invasive Ductal Carcinoma of Male Breast: A Rare Case Report

2017 ◽  
pp. 1-4
Author(s):  
Kuldeep Ananda Vaidhya ◽  
Sukesh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ductal Carcinoma ◽  
Histopathological Examination ◽  
Mucinous Carcinoma ◽  
Male Breast ◽  
Rare Entity ◽  
Infiltrating Ductal Carcinoma ◽  
Rare Case Report ◽  
Desmoplastic Stroma

Male breast carcinoma is a rare entity. Here, we present a case of mixed mucinous carcinoma i.e. composite mucinous carcinoma with infiltrating ductal carcinoma component in a 55 year old man. Patient clinically presented with a lump in his right breast. Histopathological examination of the breast mass showed tumor cells arranged in nests, cords, cribriform pattern in a mucinous stroma and a part of tumor was showing features of infiltrating ductal carcinoma with desmoplastic stroma.

scholarly journals A rare case of unruptured live second trimester ovarian ectopic pregnancy

2020 ◽  
Vol 9 (9) ◽  
pp. 3899
Author(s):  
Saroj Choudhary ◽  
Preksha T. Singh ◽  
Indra Bhati ◽  
R. K. Deora
Keyword(s):  
Ectopic Pregnancy ◽  
Rare Case ◽  
Treatment Guidelines ◽  
Histopathological Examination ◽  
First Trimester ◽  
Rare Entity ◽  
Second Trimester ◽  
Rare Presentation ◽  
Ovarian Pregnancy ◽  
Ectopic Pregnancies

Ovarian ectopic pregnancy is an extreme rare entity in all the cases of ectopic pregnancies. Before, the end of first trimester, it usually ends with rupture. It is such a unique and rare presentation that only 3% of all ectopic pregnancies are reported due to an ovarian cause. In this case report, authors have presented a patient with ovarian ectopic pregnancy which was found unruptured, live at the second trimester. The patient presented with abdominal pain and after routine check-up and ultrasound abdomen, patient was taken for an emergency explorative laparotomy and the ovarian pregnancy was excised and sent for histopathological examination, the histopathological examination further confirmed the diagnosis of the same. In some researches it has been seen that ovarian pregnancies are rising, considering that, the findings of the report may help frame future diagnostic and treatment guidelines. 

scholarly journals A parasitic myoma: clinicopathological study of a rare case

2017 ◽  
Vol 7 (1) ◽  
pp. 352
Author(s):  
Nanda J. Patil ◽  
Puja A. Pingle ◽  
Gayatri N. Patel
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Pelvic Mass ◽  
Abdominal Discomfort ◽  
Rare Entity ◽  
Imaging Studies ◽  
Fibrous Stroma ◽  
Clinicopathological Study ◽  
Pathologic Basis ◽  
Figo Classification

Leiomyoma is a benign tumour composed of smooth muscle cells with fibrous stroma and it is the commonest tumour amongst the tumours of uterus. As per FIGO classification system parasitic leiomyoma has no myometrial involvement or uterine attachment. These myomas get detached from the uterus and receive the blood supply from another source. The etiology and pathologic basis of these parasitic fibroids is not yet clearly understood. We report a rare case of parasitic myoma in a 29 years old female patient presented with abdominal discomfort and difficulty in micturition. Clinical examination and subsequent imaging studies revealed a pelvic mass. Histopathological examination of which proved it to be a parasitic myoma. Parasitic myoma is a rare entity which may be iatrogenically created after surgery particularly with morcellation technique. With increasing rates of laparoscopic procedures, surgeons should be aware of the possibility of formation of parasitic myoma and should take intraoperative precautions to minimise its formation.

scholarly journals Aggressive angiomyxoma of vulva in a young female: a rare entity with an unusual presentation

2016 ◽  
Vol 4 (1) ◽  
pp. 432
Author(s):  
Richa Jaiman ◽  
Neelabh Agrawal ◽  
Dipt Kumar ◽  
Chandrodaya Kumar ◽  
Abhishek Pathak ◽  
...  
Keyword(s):  
High Risk ◽  
Local Recurrence ◽  
Wide Local Excision ◽  
Rare Case ◽  
Histopathological Examination ◽  
Benign Neoplasm ◽  
Young Female ◽  
Aggressive Angiomyxoma ◽  
Rare Entity ◽  
Adult Females

Aggressive angiomyxoma is a rare benign neoplasm usually involving the pelvic region. It is six times more common in females than males. It occurs almost exclusively in adult females. The term aggressive signifies the neoplastic character of the blood vessels, its locally invasive nature, and the high risk of local recurrence. Here we report a rare case of an eighteen year old female, who had a vulvar swelling for over two years, which turned out to be aggressive angiomyxoma after wide local excision on histopathological examination.

scholarly journals Primary ovarian pregnancy: histopathology remains the key to confirming diagnosis setting

2017 ◽  
Vol 6 (4) ◽  
pp. 1649
Author(s):  
Priyanka Anand ◽  
Namrata Nargotra
Keyword(s):  
Abdominal Pain ◽  
Ectopic Pregnancy ◽  
Histopathological Examination ◽  
First Trimester ◽  
Accurate Diagnosis ◽  
Rare Entity ◽  
Chorionic Villi ◽  
Ovarian Pregnancy ◽  
Ovarian Stroma ◽  
History Of

Ectopic pregnancy occurs in 2% of all pregnancies. Primary ovarian pregnancy is a rare entity and accounts for only 0.15-3% of all ectopic gestations. It usually ends with rupture before the end of first trimester. The diagnosis is often made intraoperatively and confirmed histopathologically. A 23 year old female presented with severe hypogastric abdominal pain with no history of amenorrhea. She underwent a laprotomy and a right sided salpingo-oopherectomy and the excised material was sent for histopathological examination. Chorionic villi were seen within the ovarian stroma suggesting the likely possibility of an ovarian pregnancy. Ovarian pregnancy is rare; although awareness of this condition is important for reducing its associated morbidity and mortality. This highlights the importance of histopathology for the accurate diagnosis of this condition.

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