Onychomatricoma with Onychomycosis: A Case Report and Review of the Literature

2021 ◽  
pp. 1-5
Author(s):  
Thomas Novoa Gomes Jaeger ◽  
Clarissa Canella ◽  
Andreia Pizarro Leverone ◽  
Robertha Carvalho Nakamura

Onychomatricoma is a primary benign neoplasm of the nail matrix. Currently, a limited number of cases have been reported, so it is still considered a rare neoplasia. However, it is debatable if this condition is underdiagnosed and underreported. Onychomycosis is an important differential diagnosis of onychomatricoma, and sometimes, both these conditions may even coexist in the same nail. As the tumor grows, tissue microenvironment is more vulnerable to dermatophytes. Probably, the altered keratin appears to be susceptible to fungal invasion. Careful clinical assessment and dermoscopic evaluation help nailing the diagnosis. Usually, total nail avulsion is the preferred therapeutic approach when they coexist. Herein, we present a case of a middle-aged woman with onychomycosis and onychomatricoma affecting a single fingernail. The proposed therapy was oral terbinafine for 6 months followed by a conservative surgery. There were dramatic changes in dermoscopic features after fungal treatment, which, to our knowledge, have not been previously reported.

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Pankit Vachhani ◽  
Prithviraj Bose

Myeloid sarcoma represents the proliferation of myeloblasts of acute myeloid leukemia (AML) at extramedullary sites. While extramedullary involvement in AML is uncommon in itself, isolated myeloid sarcomas, that is, myeloid sarcomas without any bone marrow involvement, are extremely rare and pose a diagnostic and therapeutic challenge. Here, we present the case of a middle-aged woman with isolated myeloid sarcoma in the stomach—an organ seldom involved by this disease. Additionally, the literature on the epidemiology, diagnosis, pathology, prognosis, and therapeutic options in myeloid sarcomas has been reviewed.


2021 ◽  
Vol 14 (1) ◽  
pp. e236682
Author(s):  
Bruno Cunha ◽  
Ricardo Pacheco ◽  
Isabel Fonseca ◽  
Alexandra Borges

Solitary neurofibromas of the larynx are extremely rare, with a total of 15 cases described in the literature. Nonetheless, acquaintance with this diagnosis is important, as misdiagnoses can have negative consequences. Presenting symptoms are non-specific and depend on tumour size and location. As well-defined submucosal masses with a broad differential diagnosis, they remain a clinical and radiological challenge. While some characteristics might favour a benign nature and subtle signs might help narrow the differential diagnosis, imaging alone is not sufficient for differentiation and definitive diagnosis requires a biopsy. Complete surgical resection and long-term follow-up is indicated. We share our experience on a case of a solitary laryngeal neurofibroma in a middle-aged woman, presenting with a large well-defined paraglottic lesion.


2007 ◽  
Vol 22 (Suppl) ◽  
pp. S139 ◽  
Author(s):  
Dong-Ho Kang ◽  
Chul-Hee Lee ◽  
Soo-Hyun Hwang ◽  
In-Sung Park ◽  
Jong-Woo Han ◽  
...  

2017 ◽  
Vol 26 (2) ◽  
pp. 157-160
Author(s):  
Erik Reinertsen ◽  
Stewart G. Neill ◽  
Kambiz Nael ◽  
Daniel J. Brat ◽  
Costas G. Hadjipanayis

We report a case of fibrous meningioma with tyrosine-rich crystalloid in the frontal lobe of a middle-aged woman. The patient presented with a history of several years of worsening headaches and blurry vision, which progressed to include syncopal episodes and right-sided weakness. Imaging demonstrated a dural-based extra-axial mass arising from the right orbital roof and extending superiorly along the right frontal convexity causing right-to-left midline shift. The patient underwent a craniotomy and operative resection. Tumor architecture and cytology was similar to that of a Schwannian neoplasm, with spindled cells arranged in a fascicular architecture and displaying focal nuclear palisading. Immunohistochemical stains confirmed a diagnosis of fibrous meningioma. Light microscopy demonstrated extracellular deposits of eosinophilic crystalline material parallel to the spindled tumor cells, reminiscent of “tyrosine-rich” crystals described in salivary gland neoplasms. This is the third meningioma featuring tyrosine-rich crystalloid reported in the literature; we also summarize the previous 2 reports.


2013 ◽  
Vol 5 (6) ◽  
pp. 121
Author(s):  
Victor T.H. Yuen ◽  
Shane D. Kirby ◽  
Young Chi Woo

Paratesticular leiomyosarcomas are rare. We report two cases ofleiomyosarcoma of the epididymis diagnosed and treated in aregional community hospital in Canada in 2009 and 2010. Bothpatients were males of ages 58 and 75, respectively. They presentedwith painless masses which, on ultrasonography, appeared to besolid masses demonstrating blood flow. Each patient underwenttrans-scrotal resection of the affected epididymis. Pathologicalexamination of trans-scrotal epididymectomy specimens confirmedthe diagnosis of high-grade leiomyosarcoma. Leiomyosarcoma isan important differential diagnosis for paratesticular masses in theelderly male; the primary treatment is radical inguinal orchiectomywith high ligation of the spermatic cord.


2021 ◽  
Vol 14 (8) ◽  
pp. e242472
Author(s):  
Deshveer Babra ◽  
Suhyun Youn ◽  
Senan Devendra

Postural orthostatic tachycardia syndrome (POTS) is a common condition of orthostatic intolerance in response to changes in position. We report a case of a middle-aged woman presenting with a new onset of POTS likely due to chemotherapy for treatment of breast cancer. She was started on a trial of a beta blocker, which was effective in controlling her symptoms and heart rate. The objective of this report was to encourage clinicians to consider POTS as a differential diagnosis, while managing patients with symptoms of orthostatic intolerance.


2005 ◽  
Vol 33 (8) ◽  
pp. 412-417 ◽  
Author(s):  
Stylianos D. Megremis ◽  
Nikolaos I. Segkos ◽  
Georgios P. Gavridakis ◽  
Michael G. Mattheakis ◽  
Elias G. Kehayas ◽  
...  

2001 ◽  
Vol 115 (11) ◽  
pp. 920-922 ◽  
Author(s):  
J. A. McEwan ◽  
A. H. Mohsen ◽  
M. L. Schmid ◽  
M. W. McKendrick

Myobacterium malmoense is a non-tuberculous mycobacterium that most commonly causes pulmonary infection, particularly in patients with underlying pulmonary disease or immunodeficiency. We describe a case of Mycobacterium malmoense infection of the larynx in a previously well middle-aged woman, which has previously not been reported. The case highlights the importance of considering atypical mycobacterial infection in the differential diagnosis of laryngeal lesions.


2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Indrani S. Bhattacharya ◽  
Marc Dweck ◽  
Andrew Gardner ◽  
Mark Jones ◽  
Mark Francis

Isolated ventricular non-compaction cardiomyopathy (IVNC) is a rare, morphologically distinct primary genetic cardiomyopathy, which is now gaining prominence as an important differential diagnosis in patients presenting with cardiac failure. We describe a case report of a Nigerian male with facial dysmorphism presenting with cardiac failure. This is followed by a review of the literature with focus on the diagnosis of this condition, which may be difficult especially in non-Caucasian populations.


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