scholarly journals Ectopic Adrenocortical Tissue Attached to the Inguinal Sac in an Adult

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Yurdacan M ◽  
◽  
Turgut BC ◽  
Akinci O ◽  
Uner MB ◽  
...  
Keyword(s):  
Inguinal Hernia ◽  
Male Patient ◽  
Unusual Case ◽  
Rare Condition ◽  
Adrenal Tissue ◽  
Ectopic Adrenal Tissue

Inguinal localization of ectopic adrenal tissue is a rare condition in literature. We report an unusual case of a 28-year-old male patient with ectopic adrenocortical tissue, which was noticed coincidentally as a orangeyellowish nodule during surgery of inguinal hernia and resected for patological examination.

scholarly journals Report of a Case Diagnosed with Ectopic Adrenal Tissue in Lung

2019 ◽  
Vol 20 (-1) ◽  
pp. 259-259
Author(s):  
Berna Gul ◽  
◽  
Mustafa Karsli ◽  
Sevgi Pekcan ◽  
Tamer Altinok ◽  
...  
Keyword(s):  
Adrenal Tissue ◽  
Ectopic Adrenal Tissue

scholarly journals P144 SPERMATIC CORD LIPOSARCOMA - A VERY RARE FINDING DURING INGUINAL HERNIA SURGERY

2021 ◽  
Vol 108 (Supplement_8) ◽  
Author(s):  
Christian Gröger ◽  
Lena Kundel ◽  
Hardwig Riediger
Keyword(s):  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Condition ◽  
Minimal Invasive ◽  
Tumor Board ◽  
Fatty Tissue ◽  
Industrialized Countries ◽  
Hernia Surgery ◽  
Rare Finding ◽  
Inguinal Hernia Surgery

Abstract Aim Repair of inguinal hernia is one of the most common operations in general surgery in industrialized countries. Isolated spermatic cord liposarcoma is a very rare soft tissue tumor. Despite standardized diagnostic algorithms for inguinal hernia, it could be difficult to predict such a rare finding. Material and Methods We report a case of inadvertent inguinal liposarcoma excision during hernia surgery in a 72-year-old male patient. Except for polyposis coli there were no further illnesses. Results After a minimal invasive transabdominal preperitoneal (TAPP) repair of a symptomatic inguinal hernia last year a persistent scrotal swelling developed. Computed tomography (CT) showed a protrusion of fatty tissue into the scrotal sac. Diagnosis of scrotal hernia was made. We performed an open Lichtenstein procedure. The final pathologic examination revealed a highly differentiated liposarcoma. Staging was completed and the case was presented to a multidisciplinary sarcoma tumor board at our institution. As recommended, a inguinal reoperation was performed with wide excision. Conclusions Although a very rare condition, spermatic cord liposarcoma should be considered as a possible differential diagnosis for inguinal hernia surgery.

Management of obstructive renal failure caused by bilateral renal aspergilloma in an immunocompetent newborn

2010 ◽  
Vol 59 (3) ◽  
pp. 367-369 ◽  
Author(s):  
J. D. Martinez-Pajares ◽  
M. C. Martinez-Ferriz ◽  
D. Moreno-Perez ◽  
M. Garcia-Ramirez ◽  
S. Martin-Carballido ◽  
...  
Keyword(s):  
Renal Failure ◽  
Renal Function ◽  
Amphotericin B ◽  
Unusual Case ◽  
Bladder Exstrophy ◽  
Rare Condition ◽  
Antifungal Drugs ◽  
Fungal Colonization ◽  
Premature Babies ◽  
Obstructive Renal Failure

Fungal infection of the kidneys is a rare condition that has been reported in premature babies and in diabetic or immunocompromised adult patients. Candida spp. is the most frequent micro-organism involved. This paper reports a case of an immunocompetent newborn with a bladder exstrophy who suffered from an acute renal failure caused by bilateral renal aspergilloma (Aspergillus flavus). The newborn was treated with amphotericin B urinary tract irrigation through bilateral nephrostomy catheters, combined with liposomal amphotericin B and voriconazole therapy, which improved his renal function. However, due to persistent fungal colonization, a long antifungal treatment and permanent ureterostomies were necessary to deal with new episodes of ureterorenal obstruction. As of November 2009, despite the renal injuries, renal function had been conserved. The management of the mechanical obstruction and the choice of antifungal drugs are discussed in this unusual case.

AN UNUSUAL CASE OF NEW ONSET NEPHROPATHY IN A PATIENT OF PSORIASIS: CASE REPORT AND REVIEW OF LITERATURE

2021 ◽  
pp. 13-14
Author(s):  
VPS Punia ◽  
Apoorva Shetty ◽  
Prashant Prashant ◽  
Akash Bharti ◽  
Praveen Raman Mishra ◽  
...  
Keyword(s):  
Nephrotic Syndrome ◽  
Case Report ◽  
Male Patient ◽  
Renal Damage ◽  
Unusual Case ◽  
Review Of Literature ◽  
Immune Mediated ◽  
Different Types ◽  
Glomerular Lesions ◽  
New Onset

Psoriasis is known to cause chronic inammatory disorder of the skin through an immune mediated mechanism, it may be complicated by different types of glomerular lesions. Three different mechanisms have been implicated by which psoriasis can cause renal damage: immune-mediated renal damage, drug-related renal damage and chronic renal damage. This report presents a case of 35 years old male patient with extensive psoriasis, who presented to our hospital with nephrotic syndrome

Ectopic adrenal tissue in the cow

2000 ◽  
Vol 147 (11) ◽  
pp. 303-304 ◽  
Author(s):  
S. E. Long ◽  
I. Thomas ◽  
G. R. Pearson
Keyword(s):  
Adrenal Tissue ◽  
Ectopic Adrenal Tissue

An Unusual Case of an Odontogenic Keratocyst Associated With an Ungrafted Alveolar Cleft: A Case Report and Review of the Literature

2018 ◽  
Vol 56 (1) ◽  
pp. 110-115 ◽  
Author(s):  
Sapna Radia ◽  
Alexander C. Cash ◽  
Kanwalraj Moar
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Bone Grafting ◽  
Unusual Case ◽  
Odontogenic Keratocyst ◽  
Permanent Teeth ◽  
Treatment Modalities ◽  
Review Of The Literature ◽  
Alveolar Cleft

We describe an unusual case of an odontogenic keratocyst (OKC) associated with an ungrafted left-sided alveolar cleft in a 10-year-old male patient. There is no previous report in the literature of OKC or other dental cysts associated with an alveolar cleft. We discuss the management of the OKC prior to secondary bone grafting and present this case to highlight the difficulty in the management of OKC concurrent with grafting of the alveolar cleft site, the proximity of unerupted permanent teeth, and possible treatment modalities.

scholarly journals Adrenal heterotopic tissue in the peritoneum coincident with serous surface carcinoma

2016 ◽  
Author(s):  
Ayse Filiz Avsar ◽  
Gülin Feykan Yeğin Akçay ◽  
Emre Erdem Tas ◽  
Huseyin Levent Keskin ◽  
Aylin Yazgan
Keyword(s):  
Differential Diagnosis ◽  
Rare Condition ◽  
Cystic Mass ◽  
Fallopian Tubes ◽  
Ovarian Mass ◽  
Adrenal Tissue ◽  
Pelvic Peritoneum ◽  
Omental Caking ◽  
Heterotopic Tissue ◽  
Endocervical Canal

We report a case involving the concomitant presentation of two rare conditions: heterotopic adrenal tissue in the pelvic peritoneum and serous surface papillary carcinoma. A postmenopausal woman with an abdominal cystic mass and generalized ascites underwent laparotomy with the suspicion of ovarian carcinoma. Final histopathological analyses revealed serous surface carcinoma with metastasis to the endocervical canal, bilateral fallopian tubes, omentum, and para-aortic lymph nodes. Heterotopic adrenal tissue was also detected in the peritoneum. Serous surface carcinoma of the peritoneum should be considered in the differential diagnosis when ascites, omental caking, and peritoneal nodules are observed in a patient with or without an ovarian mass. Heterotopic adrenal tissue is another rare condition in adults and can be detected incidentally in the peritoneum.

scholarly journals Abscessed Uterine and Extrauterine Adenomyomas with Uterus-Like Features in a 56-Year-Old Woman

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Asiye Safak Bulut ◽  
Tevfik Uğur Sipahi
Keyword(s):  
Frozen Section ◽  
Benign Lesion ◽  
Broad Ligament ◽  
Transformation Theory ◽  
Pathogenetic Mechanisms ◽  
Adrenal Tissue ◽  
Uterine Malformation ◽  
Fusion Defect ◽  
Left And Right ◽  
Ectopic Adrenal Tissue

Adenomyosis, also known as endometriosis interna, is the presence of endometrial glands and stroma within the myometrium. Its localised form is called adenomyoma and mimics a leiomyoma. Rarely, adenomyomas are located outside the uterus and some of them form uterus-like masses with a thick muscle wall and an endometrium-lined central cavity. They are generally located in the ovary or broad ligament, and, although they are closely related to endometriosis, their pathogenetic mechanisms are different from each other. Müllerian duct fusion defect and subcoelomic mesenchyme transformation theory are two possible pathogenetic mechanisms for this rare entity. Here we report abscessed uterine and extrauterine adenomyomas forming uterus-like masses in the left and right broad ligament and an ectopic adrenal tissue in the left paraovarian region in a 56-year-old woman. Although there is a reported abscessed adenomyosis in the literature, this is the first abscessed extrauterine uterus-like masses with synchronous pelvic pathologies like endometriosis, leiomyomas, adenomyosis, an endometrial polyp, an endocervical polyp, and an ectopic adrenal tissue. This benign lesion gives the impression of leiomyoma, a uterine malformation, or even malignancy preoperatively. Frozen section helps in differential diagnosis.

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