scholarly journals Anal excision of perianal fibroadenoma: Expect the unexpected

2021 ◽  
Vol 9 ◽  
pp. 2050313X2110355
Author(s):  
Chiara Eberspacher ◽  
Francesco Nardi ◽  
Lisa Fralleone ◽  
Domenico Mascagni

Breast fibroadenomas are a common benign tumour in women that may need to be surgically excised. A mammary-like fibroadenoma can exceptionally be found in the pathological report after an anal polyp removal. A 60-year-old woman presented with huge anal polyp of 25 mm. It was surgically removed transanally. Histologic examination revealed a breast fibroadenoma pattern with glandular structures. Proctologist specialists must be aware that mammary-like tumours are a possible differential diagnosis for anal masses despite their rarity in the literature.

Author(s):  
Ritu Khatuja ◽  
Menka Verma ◽  
Nivedita Sarda ◽  
Dolly Chawla ◽  
Renu Gupta ◽  
...  

Leiomyoma is a most common benign tumour of uterus. But it is very rare in vagina urethral and paraurethral. There are approximately 330 case reports are available in literature and the paraurethral site is extremely uncommon. Here, we report a case of 38-year nulliparous woman presented with complain of mass coming out of vagina as well as dyspareunia. Provisional diagnosis of anterior vaginal cyst along with the differential diagnosis of paraurethral and anterior wall vaginal leiomyoma was made. Transvaginal removal of mass was done and diagnosis of paraurethral leiomyoma was confirmed by histopathology.


2000 ◽  
Vol 114 (6) ◽  
pp. 465-466 ◽  
Author(s):  
A. Kalan ◽  
A. Ahmed-Shuaib ◽  
M. Tariq

We report the first case of a lipoma originating in the fossa of Rosenmu¨ ller. Although lipomas are a common benign tumour in the body, lipomas of the nasopharynx are rare.


2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Wu Qichang ◽  
Wang Wenbo ◽  
Zheng Liangkai ◽  
Kong Hui ◽  
He Xiaoqin ◽  
...  

Background. Pregnancy with concomitant chorioangioma and placental mesenchymal dysplasia (PMD) coexisting with a normal viable fetus is very rare. The literature was reviewed to explore the incidence and genetic origin of this condition.Case. The case was first identified by prenatal ultrasonography, but the prenatal diagnosis only included chorioangioma. PMD was then confirmed during postnatal evaluation, which included gross and histologic examination of the placenta. The macroscopic and microscopic findings were consistent with concomitant chorioangioma and placental mesenchymal dysplasia during pregnancy. Genetic findings confirmed genetic similarity of the chorioangioma and vesicle-like villi with the fetus.Conclusions. The case represents a rare placental abnormality whose pathogenesis and molecular basis need further research. Detailed histologic and genetic analyses are essential for accurate and differential diagnosis.


2020 ◽  
Vol 27 (04) ◽  
pp. 870-872
Author(s):  
Afra Samad ◽  
Namra Mahmood ◽  
Arbaz Samad

We are reporting a case of tuberculosis within warthin tumour of left parotid area in a 72 years old male with findings of benign tumour with acute and chronic inflammation on FNA (Fine Needle Aspiration). Warthin tumour is a benign tumours of the salivary gland particularly parotid region. It is the second most common benign tumour. In addition the tuberculosis in a parotid gland is very rare. Further having tuberculosis within warthin tumour is quite rare.1 To best of our knowledge there is the only few cases which are being reported.


1995 ◽  
Vol 62 (2) ◽  
pp. 260-262
Author(s):  
G. Marzorati ◽  
F. Pachera ◽  
M. Caroli Costantini

Giant renal leiomyoma is a rare benign tumour with a prevalently smooth muscular component; its clinical aspect and radiological and histological aspects are described. Renal leiomyoma should always be considered in differential diagnosis of a renal mass and surgical exploration is necessary to obtain the histological evidence.


2019 ◽  
Vol 49 (3) ◽  
pp. 246-248
Author(s):  
RJ Jefferson ◽  
GD Hildebrand

Infantile haemangioma is a relatively common benign tumour which often does not require treatment. We present a case of a segmental infantile haemangioma with periocular involvement impacting on early visual development which was successfully treated with topical timolol maleate 0.5% drops in the developing world.


1945 ◽  
Vol 18 (208) ◽  
pp. 99-107 ◽  
Author(s):  
R. A. Kemp Harper ◽  
Eugene Tiscenco

1989 ◽  
Vol 103 (4) ◽  
pp. 429-431 ◽  
Author(s):  
J. D. Blanshard ◽  
D. Veitch

AbstractLipomata are the most common benign tumour of the head and neck. They may undergo a variety of changes, one of which is ossification which, although rarely seen, has a characteristic radiographic appearance. We present a case of a retropharyngeal lipoma which demonstrates ossification and discuss the features which differentiate this from an osseous lipoma. Current theories on the aetiology of lipomata and their ossification are reviewed.


HAND ◽  
1978 ◽  
Vol os-10 (3) ◽  
pp. 306-308 ◽  
Author(s):  
James G. Hoehn ◽  
Daniel T. Davis

Fibrous xanthomas* of the digital tendon sheath system are a common benign tumour. The varying recurrence rates cited in the literature have usually been attributed to inadequate surgical excision. However, Boyes (1964) has suggested “seeding” as a possible mechanism to explain persistence of the tumour. Our case of multiple fibrous xanthomas at different levels in a single digital sheath system is presented as an example of “seeding” along the tendon sheath.


2014 ◽  
Vol 4 (1) ◽  
pp. 47-51
Author(s):  
AK Yadav ◽  
PY Feng ◽  
XC Chen ◽  
LJ Feng

We present a case of 61years old female, clinical manifestations of this entity, including left lumber continuous pain and discomfort with numbness at left gluteal region for 2 years. Pain had increase since one week with radicular pain in left leg. MRI study was performed with 3.0T unit (siemen) and revealed an oval shape mass behind the L3 vertebra, suggesting differential diagnosis of Neurilemoma or Ependymoma. The patient underwent surgical L3 laminectomy and total excision of the tumor. Pathological report confirmed diagnosis of Neurilemoma.#DOI: http://dx.doi.org/10.3126/njr.v4i1.11369 Nepalese Journal of Radiology, Vol.4(1) 2014: 47-51 


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