scholarly journals Cystosarcoma Phyllodes Metastatic to the Mandible: Report of a Rare Case and Literature Review

2003 ◽  
Vol 82 (5) ◽  
pp. 380-381 ◽  
Author(s):  
Jonathan B. Staton ◽  
Thomas H. Costello ◽  
F. Daniel Donovan ◽  
Robert E. Laster
Keyword(s):  
Literature Review ◽  
Breast Neoplasm ◽  
Breast Tumor ◽  
Rare Case ◽  
Phyllodes Tumor ◽  
Malignant Potential ◽  
Cystosarcoma Phyllodes ◽  
The Third

Cystosarcoma phyllodes is a rare breast tumor with variable malignant potential. Metastasis has been reported in a small percentage of cases. We describe the case of a 52-year-old woman who developed a large facial tumor 1 year after she had undergone a mastectomy fora rapidly enlarging breast neoplasm. The facial lesion was found to be a malignant cystosarcoma phyllodes metastatic to the mandible, and the patient died shortly after diagnosis. To our knowledge, this patient represents only the third reported case of a phyllodes tumor metastatic to the mandible.

scholarly journals Diagnosis and management of congenital epulis of new-born: a rare case report and literature review

2015 ◽  
Vol 1 (1) ◽  
pp. 80
Author(s):  
Bacem A. E. Ottoman
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Pediatric Oncology ◽  
Rare Case ◽  
Spontaneous Regression ◽  
Malignant Potential ◽  
New Born ◽  
Rare Case Report ◽  
Congenital Epulis ◽  
Neonatal Lesions

<p class="abstract">The congenital epulis of new-born is a rare disease of idiopathic etiology and lineage. The literature recorded spontaneous regression of some cases. This finding rendered skeptical questions about its neoplastic nature and posed some speculations about hormonal influences, towards the end of pregnancy, on the growth of the lesion. No malignant potential has been ever reported. Surgery is indicated if the lesion grossly interferes with breast feeding. This paper reports an established diagnosis of congenital epulis of new-born, which was excised surgically with no evidence of recurrence hitherto. </p><p><strong>Keywords: </strong>Congenital epulis, Neonatal lesions, Mucosal swellings, Pediatric oncology</p>

Spinal Epidermoid Cyst in a Child- An Experience with a Rare Case

2019 ◽  
Vol 2 (2) ◽  
pp. 80-83
Author(s):  
P Chaudhary ◽  
BP Shrestha ◽  
GK Khanal ◽  
R Maharjan ◽  
RPS Kalawar ◽  
...  
Keyword(s):  
Spina Bifida ◽  
Literature Review ◽  
Rare Case ◽  
Benign Neoplasm ◽  
Spinal Tumors ◽  
Dermal Sinus ◽  
Epidermoid Cysts ◽  
The Third ◽  
Embryonic Life ◽  
Common Etiology

Epidermoid cysts are rare benign neoplasm accounting for less than 1% of all intra-spinal tumors. Congenital epidermis cysts are frequently found with syringomyelia, dermal sinus and spina bifida. Most common etiology for an acquired cyst is repeated lumbar puncture. Congenital epidermoid cysts, often associated with other spinal dysraphisms, are caused by the anomalous implantation of ectodermalcells during closure of the neural tube between the third and fifth week of embryonic life. This is a very rare case. With all these characteristics and literature review, we report this case for its rarity and unique characteristics in this part of world (Nepal). These patients commonly present late to the hospital.

scholarly journals Bone metastasis from malignant phyllodes of the breast

2019 ◽  
Vol 7 (11) ◽  
pp. 4364
Author(s):  
Daniel Oktavianus Dau ◽  
I. Wayan Sudarsa
Keyword(s):  
Case Report ◽  
Bone Metastasis ◽  
Breast Tumor ◽  
Benign Tumor ◽  
Phyllodes Tumor ◽  
Breast Tumors ◽  
Upper Arm ◽  
Malignant Phyllodes Tumor ◽  
Cystosarcoma Phyllodes ◽  
The Right

Cystosarcoma phyllodes was described first in 1838 and originally was considered to be a benign tumor. It was not until 1931 that metastasis from a cystosarcoma phyllodes was reported. The incidence of cystosarcoma phyllodes is estimated to be 0.3% to 0.9% of all breast tumors. Sites most commonly affected by metastases are the lungs and bones. We present a case report  29-year old female patient presented with a voluminous breast mass at both of them  which was completely resected. The right side presented of malignant phyllodes and the left side is borderline phyllodes. Six months later, both of her legs became paralyzed and accompanied by swelling over her right upper arm. Biopsy was performed, and the diagnosis was metastatic malignant phyllodes tumor. Histologic review of the breast tumor revealed stromal overgrowth.

scholarly journals Giant malignant phyllodes tumor of the breast: A rare case report and literature review

2016 ◽  
Vol 12 (1) ◽  
pp. 121-124 ◽  
Author(s):  
MIN LIU ◽  
SHUO YANG ◽  
BIN LIU ◽  
LIANG GUO ◽  
XUEYING BAO ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Phyllodes Tumor ◽  
Malignant Phyllodes Tumor ◽  
Rare Case Report

Popliteal nodal metastasis from squamous cell cancer of the foot. Case report and literature review

2019 ◽  
pp. 1-2
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Literature Review ◽  
Squamous Cell ◽  
Rare Case ◽  
Squamous Cell Cancer ◽  
Cell Cancer ◽  
Nodal Metastasis ◽  
Regional Disease ◽  
The Right

We report a very rare case of squamous cell cancer of the right foot which had metastasize to the ipsilateral popliteal lymph node after initial diagnosis and treatment for the loco-regional disease.

Penile Lymphoepithelioma-Like Carcinoma: A Rare Case With PD-L1 Expression

2021 ◽  
pp. 106689692098834
Author(s):  
Raquel Machado-Neves ◽  
Bernardo Teixeira ◽  
Elsa Fonseca ◽  
Pedro Valente ◽  
Joaquim Lindoro ◽  
...  
Keyword(s):  
Human Papillomavirus ◽  
Tumor Cells ◽  
Rare Case ◽  
Malignant Tumors ◽  
Squamous Cell Carcinomas ◽  
The Third ◽  
The Past ◽  
First Case ◽  
Lymphoplasmacytic Infiltrate

Most malignant tumors of the penis are squamous cell carcinomas (SCC), being divided in 2 groups, one human papillomavirus (HPV)-related and another non-HPV-related, with lymphoepithelioma-like carcinoma (LELC) being one of the rarest HPV-related SCC. In this article, we report a case of a 50-year-old man who presented testicular swelling and pain for the past 3 months. A penile mass was identified, and the patient was submitted to a total penectomy. The penectomy specimen showed an ulcerated lesion at the glans reaching the cavernous bodies. Microscopic examination showed undifferentiated epithelial cells with syncytial growth pattern mix with a dense lymphoplasmacytic infiltrate, consistent with LELC. The tumor cells expressed p16 and all 3 different clones of PDL1 (22C3, SP263, and SP142). The patient is alive and well with a follow-up of 3 months. To our knowledge, this is the third LELC of the penis reported in literature and the first case reported with PDL1 expression.

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