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1.
Mod Pathol ; 33(12): 2499-2506, 2020 12.
Article in English | MEDLINE | ID: mdl-32620918

ABSTRACT

Estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor-2 (HER2) status provide clinical utility in guiding therapeutic decision-making in metastatic breast cancer (BC). Increasing data have shown substantial differences between the receptor profiles of primary BCs and their paired metastases. In this study, we provide a large single center cohort to assess the frequency of receptor conversion in metastatic BC. The overall discordant rates were 18.3%, 40.3%, and 13.7% for ER, PR, and HER2, respectively. The discordance was significantly higher for PR when compared with ER and HER2. The conversion occurred significantly as a switch from positive to negative receptor status when compared with that from negative to positive for all three receptors. Semiquantitative analyses revealed a significantly decreased expression of both ER (25%) and PR (57%) in the metastases. There was a higher rate of PR discordance in bone metastases when comparing to other common organs of relapse. Furthermore, in the subset of patients with a single primary and multiple distant metastases, the discordant rates among the distant sites were 27.5%, 39.4%, and 14.3% for ER, PR, and HER2, respectively. A positive ER status, be it in primary or metastatic BC, was associated with a prolonged metastasis-free survival when compared with ER-negative primary tumors without conversion. Furthermore, a positive ER status in metastatic BC regardless of primary was associated with a superior overall survival when compared with an ER-negative tumor without conversion. Thus, receptor conversion is a frequent event in the course of BC progression, and can also be seen between different metastatic sites. Moreover, some conversions are of prognostic significance. The findings may reflect tumor heterogeneity, sampling or treatment effect, but may also indicate alteration in tumor biology. Repeat biomarker testing is warranted in making appropriate treatment plans in the pursuit of precision medicine.


Subject(s)
Biomarkers, Tumor/genetics , Breast Neoplasms/genetics , Receptor, ErbB-2/genetics , Receptors, Estrogen/genetics , Receptors, Progesterone/genetics , Alabama , Breast Neoplasms/mortality , Breast Neoplasms/pathology , Breast Neoplasms/therapy , Female , Genetic Predisposition to Disease , Humans , Neoplasm Metastasis , Phenotype , Prognosis
2.
Cureus ; 10(10): e3419, 2018 Oct 05.
Article in English | MEDLINE | ID: mdl-30542633

ABSTRACT

Leiomyomas are benign tumors of smooth muscle origin. They are most commonly found in the uterus, but cutaneous leiomyomas may be occasionally present in the extremities and cause pain secondary to mass effect. Few studies have reported leiomyoma of the foot, and leiomyoma of the heel is particularly rare. We present a case of a 41-year-old female who presented to our clinic for a tender nodule on the posterior aspect of her right heel. The tumor was surgically excised and biopsied revealing cutaneous leiomyoma.

3.
Cardiovasc Pathol ; 37: 26-29, 2018.
Article in English | MEDLINE | ID: mdl-30223140

ABSTRACT

A 73-year-old woman with a past medical history of hypertension suffered a cardiac arrest. After successful resuscitation, she was hypotensive and tachycardic and the ECG showed ST elevation in the inferior and lateral precordial leads. Coronary angiography did not show evidence of obstructive coronary artery disease. A bedside echocardiogram demonstrated a large pericardial effusion with signs of cardiac tamponade. The echocardiogram and subsequent aortic root angiography did not reveal evidence of dissection. Pericardiocentesis removed 700 cc of bloody fluid with relief of tamponade. A few minutes later the patient again arrested. Fluid was again drained but she suffered recurrent hemodynamic collapse and could not be resuscitated. Autopsy revealed a small transmural myocardial infarction with external rupture and hemopericardium. There was only mild coronary artery disease without evidence of plaque rupture. This case illustrates that mild coronary artery disease and a small myocardial infarction can lead to catastrophic mechanical complications.


Subject(s)
Heart Rupture, Post-Infarction/etiology , Myocardium/pathology , ST Elevation Myocardial Infarction/complications , Aged , Cardiac Tamponade/etiology , Coronary Angiography , Echocardiography , Electrocardiography , Fatal Outcome , Female , Heart Rupture, Post-Infarction/pathology , Heart Rupture, Post-Infarction/therapy , Humans , Pericardial Effusion/etiology , Pericardiocentesis , Recurrence , ST Elevation Myocardial Infarction/pathology
4.
Cureus ; 10(6): e2797, 2018 Jun 13.
Article in English | MEDLINE | ID: mdl-30116676

ABSTRACT

The number of total knee arthroplasties (TKAs) being performed annually is steadily rising. Recommendations for clinical follow-up guidelines following these arthroplasties is controversial, with no strict guidelines for long-term follow up. Although a few case series exist which identify a minority of patients who require revision TKA for aseptic loosening or pain more than 15 years after index surgery, no published studies have yet described these patients or the pathology present at the time of surgery in detail. We present the case of a patient who underwent revision TKA for pain and instability that developed 17 years after index surgery. Postoperative pathology revealed foreign body giant cell reaction of the tissue surrounding the previous implant. This case of revision after more than 17 years attempts to improve our understanding of long-term reactions to implants and highlights the necessity of long-term follow up in patients with TKA. It is one of the longest follow-ups of TKA reporting long-term anatomic changes at the bone cement interphase and around the implant.

5.
Int J Surg Pathol ; 26(5): 440-447, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29390927

ABSTRACT

We present a case of a malignant Ewing-like neoplasm of the parotid gland in a 20-year-old woman with an EWSR1-KLF15 gene fusion that presented with pulmonary metastasis. Despite the fact that the tumor was essentially immunohistochemically negative for keratins, p63, and p40, we interpret this neoplasm as an unusual form of a high-grade myoepithelial carcinoma based on its focal plasmacytoid cytology, chondromyxoid matrix, SOX10, S100 protein, and calponin expression, and the knowledge that the EWSR1-KLF15 gene fusion has, to date, only been identified in 2 tumors, both myoepithelial carcinomas of the kidney. We also present a cytogenetic analysis of this unusual tumor. This "Ewing-like myoepithelial carcinoma" initially did not respond to 2 cycles of ifosfamide and etoposide alternated with a cycle of cytoxan, adriamycin, and vincristine, a standard regimen for Ewing sarcoma. Subsequent oral pazopanib therapy did result in a reduction of the patient's pulmonary and nodal disease.


Subject(s)
Carcinoma/genetics , Myoepithelioma/genetics , Oncogene Proteins, Fusion/genetics , Parotid Gland/pathology , Sarcoma, Ewing/genetics , Adult , Carcinoma/diagnostic imaging , Carcinoma/pathology , Carcinoma/surgery , Female , Humans , Kruppel-Like Transcription Factors/genetics , Lymph Nodes/pathology , Lymph Nodes/surgery , Lymphatic Metastasis , Myoepithelioma/diagnostic imaging , Myoepithelioma/pathology , Myoepithelioma/surgery , Neck , Nuclear Proteins/genetics , Parotid Gland/diagnostic imaging , Parotid Gland/surgery , Positron Emission Tomography Computed Tomography , RNA-Binding Protein EWS/genetics , Sarcoma, Ewing/diagnostic imaging , Sarcoma, Ewing/pathology , Sarcoma, Ewing/surgery , Young Adult
6.
Int J Surg Pathol ; 26(2): 126-134, 2018 Apr.
Article in English | MEDLINE | ID: mdl-28954565

ABSTRACT

The diagnostic distinction between endometrial serous carcinoma (ESC) and endometrial clear-cell carcinoma (CCC) may occasionally be problematic, and one potentially contributing factor is the finding of clear cells in otherwise classic cases of ESC. This study aimed to define the frequency of this finding and comparatively assessed the immunophenotype of the clear cells. A review of 56 cases of ESC identified 8 (14.28%) with clear cells, representing 1% to 20% (median 7.5) of tumoral volume in these cases. In only 3 cases were clear cells discernible at low (×20) magnification. There was no significant difference in stage distribution or age between ESC patients with and without clear cells. The immunophenotypes of ESC-associated clear cells (group 1) were compared with foci of conventional ESC on another tissue block within the same case (group 2; n = 8) as well as a randomly selected cohort of CCC cases (group 3; n = 8). Groups 1 and 2 showed no significant differences regarding p53, ER, PR, Napsin-A, p504S, and hepatocyte nuclear factor 1ß (HNF1ß) expression, or regarding mitotic indices or Ki67 proliferation rate. In contrast, group 1 cases showed an immunophenotypic profile that was notably different from that of group 3 cases, with the former showing statistically significantly higher/more frequent expression of ER, PR, Ki67, and p53 and lower/less frequent expression of Napsin-A, p504S, and HNF1ß. We conclude that clear-cell change is seen in 14% of ESCs and is discernible at low magnification in only 5%; these areas show an immunophenotype that is essentially identical to the associated background conventional ESC and are phenotypically dissimilar to CCC.


Subject(s)
Adenocarcinoma, Clear Cell/pathology , Biomarkers, Tumor/analysis , Cystadenocarcinoma, Serous/pathology , Endometrial Neoplasms/pathology , Adenocarcinoma, Clear Cell/diagnosis , Aged , Aged, 80 and over , Cystadenocarcinoma, Serous/diagnosis , Endometrial Neoplasms/diagnosis , Female , Humans , Immunohistochemistry , Middle Aged
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