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1.
BMJ Case Rep ; 17(9)2024 Sep 16.
Article in English | MEDLINE | ID: mdl-39284682

ABSTRACT

Intramuscular haemangiomas (IH) are rare lesions, accounting for less than 1% of all haemangiomas. This article presents the case of a woman in her 40s with a swelling in her left cheek. CT revealed an intramuscular lesion within the masseter, suggestive of a venous malformation. Surgical treatment was carried out with intraoral access to the lesion, allowing for complete removal, resulting in temporary swelling and trismus. There was no facial paralysis. We discuss information on IH in the head and neck and their surgical approaches.


Subject(s)
Hemangioma, Cavernous , Masseter Muscle , Humans , Masseter Muscle/pathology , Masseter Muscle/surgery , Female , Hemangioma, Cavernous/surgery , Hemangioma, Cavernous/diagnostic imaging , Hemangioma, Cavernous/pathology , Adult , Muscle Neoplasms/surgery , Muscle Neoplasms/diagnostic imaging , Muscle Neoplasms/pathology , Tomography, X-Ray Computed
2.
J Cutan Pathol ; 46(8): 603-608, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31006896

ABSTRACT

Intramuscular hemangioma (IMH) represents less than 1% of all hemangiomas. In the head and neck region, it occurs mostly in the masseter, temporalis and sternocleidomastoid muscles. Despite its infiltrative growth pattern and several worrisome histological features, such as increased mitotic activity, plumpness of the nuclei, intraluminal papillary projections or perineural infiltration, the lesion is benign, and complete surgical excision is the preferred treatment for such oral lesions. Herein, we report three rare cases of IMH in the tongue and lip, discuss the clinical and histological aspects, and review the literature regarding this lesion.


Subject(s)
Hemangioma , Mouth Neoplasms , Muscle Neoplasms , Aged , Female , Hemangioma/metabolism , Hemangioma/pathology , Hemangioma/surgery , Humans , Male , Middle Aged , Mouth Neoplasms/metabolism , Mouth Neoplasms/pathology , Mouth Neoplasms/surgery , Muscle Neoplasms/metabolism , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery
3.
Clin Transl Oncol ; 21(9): 1240-1249, 2019 Sep.
Article in English | MEDLINE | ID: mdl-30712233

ABSTRACT

PURPOSE: Sphingosine 1 phosphate (S1P), S1P receptors (S1PRs) and their signaling pathways play an important role in the fate of cancer cells. The expression pattern of S1PR subtypes (S1PR1-S1PR5) may alter in cancer development stages, depending on the origin and the pathologic features of tumors. The present study aimed to examine the relationship between plasma S1P levels and the expression of S1PR subtypes in bladder tumors. METHODS/PATIENTS: These changes were evaluated in terms of the pathologic grades and stages of human bladder cancer samples. For this, tumor biopsies from 41 new bladder cancer patients as well as 26 normal-looking bladder tissues were collected and processed for immunohistochemistry (IHC) and quantitative real-time RT-PCR of S1PR subtypes. Plasma S1P level was measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS). RESULTS: The results show that tissue S1PR1, S1PR2 and S1PR3 are over-expressed in all tumors regardless of their pathological grade (~ 3, ~ 6 and ~ 104 folds, respectively). These results were corroborated by IHC data showing accumulation of S1PR subtypes 1 and 2 in the tissues. Plasma S1P in the plasma samples from patients was in the range of control samples (Controls; 256 ± 47; patients, 270 ± 41). CONCLUSIONS: Overexpression of S1PR1, S1PR2 and S1PR3 in bladder tumor biopsies which were corroborated with the pathological grades and stages may suggest that S1PR profile in tumor biopsies is a promising marker in the diagnosis of bladder carcinoma.


Subject(s)
Biomarkers, Tumor/metabolism , Carcinoma, Transitional Cell/metabolism , Muscle Neoplasms/metabolism , Sphingosine-1-Phosphate Receptors/metabolism , Urinary Bladder Neoplasms/metabolism , Biomarkers, Tumor/genetics , Carcinoma, Transitional Cell/genetics , Carcinoma, Transitional Cell/pathology , Carcinoma, Transitional Cell/surgery , Case-Control Studies , Follow-Up Studies , Gene Expression Regulation, Neoplastic , Humans , Muscle Neoplasms/genetics , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery , Prognosis , Sphingosine-1-Phosphate Receptors/genetics , Urinary Bladder Neoplasms/genetics , Urinary Bladder Neoplasms/pathology , Urinary Bladder Neoplasms/surgery
6.
Bol Med Hosp Infant Mex ; 75(1): 31-40, 2018.
Article in Spanish | MEDLINE | ID: mdl-29652875

ABSTRACT

Background: Imaging studies, particularly simple and contrast-enhanced tomography, constitute the first diagnostic approach to detect recurrence of musculoskeletal tumors. The aim of the present retrospective study was to demonstrate the usefulness of scintigraphy plus SPECT/CT (single photon emission computed tomography) with thallium-201 (201Tl) in the evaluation of malignant musculoskeletal tumors with suspicion of recurrence or metastatic disease. Methods: Eight weeks after the last therapy, 72 scintigraphy and SPECT/CT studies were performed to assess regional recurrence and metastatic disease in 42 patients with different types of malignant musculoskeletal tumors, such as osteosarcoma, Ewing's sarcoma, rhabdomyosarcoma, retinoblastoma, synovial sarcoma, and Wilms tumor at the Hospital Infantil de México Federico Gómez. The positive predictive value (PPV) and the confidence interval of the scintigraphy and SPECT/CT were calculated when compared with the results of the histopathological analysis and the clinical and radiological follow-up for the identification of recurrence. Results: Scintigraphy was abnormal in 30 (71.4%) of the 42 patients; 33 lesions (30 patients) were detected by scintigraphy and 25 lesions (21 patients) by chest X-ray and tomography of two regions. The SPECT/CT was performed on 30 patients, where 12 lesions were detected in addition to the planar scintigraphy. Scintigraphy showed a PPV of 82%; SPECT/CT, 100%. Conclusion: 201Tl-scintigraphy can be considered as an adequate study to identify the sites of tumor viability with a high degree of diagnostic certainty combined with the SPECT/CT technique.


Introducción: Los estudios de imagen, como la tomografía simple y contrastada, son la primera aproximación diagnóstica para detectar la recurrencia de tumores musculoesqueléticos. El objetivo de este estudio retrospectivo fue demostrar la utilidad de la gammagrafía acoplada a tomografía computarizada por emisión de fotón único (SPECT/CT) con talio-201(201Tl) en la valoración de tumores musculoesqueléticos malignos con sospecha de recurrencia o enfermedad metastásica. Métodos: Se realizaron 72 estudios gammagráficos y de SPECT/CT para la valoración de la recurrencia locorregional y a distancia, al menos 8 semanas tras la última terapia, en 42 pacientes con diferentes tipos de tumores musculoesqueléticos malignos, como osteosarcoma, sarcoma de Ewing, rabdomiosarcoma, retinoblastoma, sarcoma sinovial y tumor de Wilms en el Hospital Infantil de México. Se calcularon el valor predictivo positivo (VPP) y el intervalo de confianza del gammagrama y de la SPECT/CT en comparación con el resultado del análisis histopatológico y el seguimiento clínico y radiológico para identificar la recurrencia. Resultados: La gammagrafía fue anormal en 30 (71.4%) de los 42 pacientes. Se detectaron 33 lesiones (30 pacientes) por gammagrafía y 25 (21 pacientes) por telerradiografía de tórax y tomografía de dos regiones. La SPECT/CT se realizó en 30 pacientes y se detectaron 2 lesiones adicionales al rastreo planar. El VPP con la gammagrafía fue del 82%, y con la SPECT/CT, del 100%. Conclusión: La gammagrafía con 201Tl puede considerarse un estudio adecuado para identificar los sitios de viabilidad tumoral, con alto grado de certeza diagnóstica al complementar con SPECT/CT.


Subject(s)
Bone Neoplasms/diagnostic imaging , Muscle Neoplasms/diagnostic imaging , Single Photon Emission Computed Tomography Computed Tomography/methods , Adolescent , Bone Neoplasms/pathology , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Male , Mexico , Muscle Neoplasms/pathology , Neoplasm Recurrence, Local , Predictive Value of Tests , Radionuclide Imaging/methods , Retrospective Studies , Thallium Radioisotopes/administration & dosage
7.
Bol. méd. Hosp. Infant. Méx ; 75(1): 31-40, ene.-feb. 2018. tab, graf
Article in Spanish | LILACS | ID: biblio-951289

ABSTRACT

Resumen Introducción: Los estudios de imagen, como la tomografía simple y contrastada, son la primera aproximación diagnóstica para detectar la recurrencia de tumores musculoesqueléticos. El objetivo de este estudio retrospectivo fue demostrar la utilidad de la gammagrafía acoplada a tomografía computarizada por emisión de fotón único (SPECT/CT) con talio-201(201Tl) en la valoración de tumores musculoesqueléticos malignos con sospecha de recurrencia o enfermedad metastásica. Métodos: Se realizaron 72 estudios gammagráficos y de SPECT/CT para la valoración de la recurrencia locorregional y a distancia, al menos 8 semanas tras la última terapia, en 42 pacientes con diferentes tipos de tumores musculoesqueléticos malignos, como osteosarcoma, sarcoma de Ewing, rabdomiosarcoma, retinoblastoma, sarcoma sinovial y tumor de Wilms en el Hospital Infantil de México. Se calcularon el valor predictivo positivo (VPP) y el intervalo de confianza del gammagrama y de la SPECT/CT en comparación con el resultado del análisis histopatológico y el seguimiento clínico y radiológico para identificar la recurrencia. Resultados: La gammagrafía fue anormal en 30 (71.4%) de los 42 pacientes. Se detectaron 33 lesiones (30 pacientes) por gammagrafía y 25 (21 pacientes) por telerradiografía de tórax y tomografía de dos regiones. La SPECT/CT se realizó en 30 pacientes y se detectaron 12 lesiones adicionales al rastreo planar. El VPP con la gammagrafía fue del 82%, y con la SPECT/CT, del 100%. Conclusión: La gammagrafía con 201Tl puede considerarse un estudio adecuado para identificar los sitios de viabilidad tumoral, con alto grado de certeza diagnóstica al complementar con SPECT/CT.


Abstract Background: Imaging studies, particularly simple and contrast-enhanced tomography, constitute the first diagnostic approach to detect recurrence of musculoskeletal tumors. The aim of the present retrospective study was to demonstrate the usefulness of scintigraphy plus SPECT/CT (single photon emission computed tomography) with thallium-201 (201Tl) in the evaluation of malignant musculoskeletal tumors with suspicion of recurrence or metastatic disease. Methods: Eight weeks after the last therapy, 72 scintigraphy and SPECT/CT studies were performed to assess regional recurrence and metastatic disease in 42 patients with different types of malignant musculoskeletal tumors, such as osteosarcoma, Ewing's sarcoma, rhabdomyosarcoma, retinoblastoma, synovial sarcoma, and Wilms tumor at the Hospital Infantil de México Federico Gómez. The positive predictive value (PPV) and the confidence interval of the scintigraphy and SPECT/CT were calculated when compared with the results of the histopathological analysis and the clinical and radiological follow-up for the identification of recurrence. Results: Scintigraphy was abnormal in 30 (71.4%) of the 42 patients; 33 lesions (30 patients) were detected by scintigraphy and 25 lesions (21 patients) by chest X-ray and tomography of two regions. The SPECT/CT was performed on 30 patients, where 12 lesions were detected in addition to the planar scintigraphy. Scintigraphy showed a PPV of 82%; SPECT/CT, 100%. Conclusion: 201Tl-scintigraphy can be considered as an adequate study to identify the sites of tumor viability with a high degree of diagnostic certainty combined with the SPECT/CT technique.


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Male , Bone Neoplasms/diagnostic imaging , Muscle Neoplasms/diagnostic imaging , Single Photon Emission Computed Tomography Computed Tomography/methods , Bone Neoplasms/pathology , Thallium Radioisotopes/administration & dosage , Radionuclide Imaging/methods , Predictive Value of Tests , Retrospective Studies , Follow-Up Studies , Muscle Neoplasms/pathology , Mexico , Neoplasm Recurrence, Local
8.
J Craniofac Surg ; 29(1): e96-e97, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28968320

ABSTRACT

Lipomas are benign tumors of mature adipocytes unusual in the oral and maxillofacial region. The average size of cheek lipomas in the literature ranges from 1.5 to 2.5 cm, with the maximum size of 5 cm. Their etiology remains unclear. Lipomas present, clinically, as well circumscribed, slow growing, painless masses, usually treated by complete excision. The aim of this paper is to present a 78-year-old Caucasian male patient with a huge cheek lipoma compromising facial esthetics and treated through an intraoral excision. Postoperative period was uneventful with no signs of recurrence. Concluding, the intraoral approach is a relatively simple technique that should be taken into account when considering the surgical removal of cheek lipomas.


Subject(s)
Cheek , Lipoma , Mouth Neoplasms , Muscle Neoplasms , Oral Surgical Procedures/methods , Aged , Cheek/pathology , Cheek/surgery , Dissection/methods , Humans , Lipoma/pathology , Lipoma/surgery , Male , Mouth Neoplasms/pathology , Mouth Neoplasms/surgery , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery , Treatment Outcome , Tumor Burden
9.
Clin Transl Oncol ; 20(7): 899-905, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29159793

ABSTRACT

PURPOSE: To report the outcomes of a cohort of very elderly muscle-invasive bladder cancer (MIBC) patients treated with contemporary 3D-conformal radiation therapy (3D-CRT) with or without concurrent chemotherapy, after transurethral resection of bladder tumor (TURBT). METHODS: From February 2010 to January 2014, a total of 41 patients older than 75 years, with T2-3 N0-1 high-grade MIBC, a Karnofsky index (KI) of at least 90% and/or a Barthel scale score of at least 95, were treated with TURBT followed by radiotherapy (RT) with or without chemotherapy, and were prospectively followed-up. RESULTS: The mean age of patients was 82 years (range 76-88). Median follow-up was 47 months for surviving patients. Mean Charlson Comorbidity Index (CCI) score was 5 points. 28 patients (68.29%) were T2N0. All received 3D-CRT to a mean dose of 60 Gy (range 48.6-66 Gy), and chemotherapy was delivered to 34 patients (83%). Cause-specific survival (CSS) was 86 and 78.8% at 1 and 5 years, respectively. Patients achieving a complete response lived longer (48 vs 14 m, p = 0.036) than those with a progressive disease, who were more likely to die from cancer than from other causes (HR 3.865, IC95% 1.562-9.562). Dead patients had a longest treatment time (mean 56.78 vs 48.91 days, p = 0.019) than survivors. CONCLUSION: RT with contemporary 3D-CRT techniques after TURBT for MIBC in elderly patients is feasible and well-tolerated. Achieving a maximal response and shortening the total radiation treatment time may improve outcomes and quality of life.


Subject(s)
Muscle Neoplasms/radiotherapy , Neoplasm Recurrence, Local/radiotherapy , Quality of Life , Radiotherapy, Conformal/mortality , Urinary Bladder Neoplasms/radiotherapy , Aged , Aged, 80 and over , Cohort Studies , Female , Follow-Up Studies , Humans , Male , Muscle Neoplasms/pathology , Neoplasm Recurrence, Local/pathology , Organ Sparing Treatments , Prognosis , Survival Rate , Urinary Bladder Neoplasms/pathology
10.
Rev Peru Med Exp Salud Publica ; 31(3): 431-6, 2014.
Article in Spanish | MEDLINE | ID: mdl-25418639

ABSTRACT

OBJECTIVES: To assess the frequency and factors associated with parametrial involvement (PI) in patients with cervical cancer IB1 who underwent radical hysterectomy (RH) at the National Institute of Neoplastic Diseases in Peru. MATERIALS AND METHODS: Cross-sectional study of 214 patients with cervical cancer IB1 undergoing RH with pelvic lymphadenectomy between 2007 and 2012. The population was compared with and without clinicopathological variables associated with PI such as age, tumor size, depth of infi histological grade and pelvic lymph node involvement. RESULTS: Ten patients (4.6%) had PI. Multivariate analysis showed that the depth of invasion (OR 8.37, 95% CI 1.24- 56.41, p=0.029) and pelvic node involvement (OR 18.03; 95% CI 3.30-98.44, p=0.001) were all independent predictors of PI. The presence of tumor size = 2 cm, invasion = 10 mm, absence of lymphovascular permeation and absence of nodal involvement identifi 97 patients at low risk of PI, none of whom had PI pathology. CONCLUSIONS: We confi the low frequency of PI in the cervical cancer IB1 subgroup and its association with the depth of invasion and lymph node involvement suggested in previous studies. This information will allow the identifi of a subgroup of patients at low risk of PI for less radical surgery in our institution.


Subject(s)
Hysterectomy , Muscle Neoplasms/pathology , Pelvic Floor , Uterine Cervical Neoplasms/pathology , Uterine Cervical Neoplasms/surgery , Adult , Aged , Cross-Sectional Studies , Female , Humans , Hysterectomy/methods , Middle Aged , Neoplasm Invasiveness , Peru , Young Adult
11.
Einstein (Säo Paulo) ; 12(3): 351-354, Jul-Sep/2014. graf
Article in Portuguese | LILACS | ID: lil-723934

ABSTRACT

A síndrome do impacto é definida pela colisão dos tendões dos músculos que formam o manguito rotador contra o arco coracoacromial. Vários fatores concorrem para essa doença e são classificados como estruturais ou funcionais. Os primeiros são alterações do arco coracoacromial, úmero, bursa e manguito rotador; os fatores funcionais estão relacionados com o mecanismo de elevação do membro superior, por meio da atividade sincronizada e equilibrada entre o manguito rotador e os músculos da cintura escapular. Os autores relatam aqui, o caso de um lipoma parosteal do úmero proximal, situado entre os ventres musculares do deltoide, redondo menor e infraespinhal ocasionando os sinais clínicos da síndrome do impacto. Trata-se de uma ocorrência rara, caracterizada como uma causa estrutural para o desencadeamento dessa sintomatologia.


The impingement syndrome is defined by the compression of the rotator cuff tendons against the coracoacromial arch. Several factors contribute to this condition and they are classified as structural or functional factors. The former are changes in the coracoacromial arch, proximal humerus, bursa and rotator cuff, and the latter are related to the mechanism of the upper limb by means of synchronized activity and balanced between the rotator cuff and scapular girdle muscles. The authors report here a case of parosteal lipoma of the proximal humerus, located between the muscles deltoid, teres minor and infraspinatus causing clinical signs of impingement. It is a rare occurrence, characterized as a structural cause for the onset of this symptom.


Subject(s)
Aged, 80 and over , Female , Humans , Deltoid Muscle , Lipoma/complications , Muscle Neoplasms/complications , Shoulder Impingement Syndrome/etiology , Deltoid Muscle/pathology , Deltoid Muscle/surgery , Lipoma/pathology , Lipoma/surgery , Magnetic Resonance Imaging , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery , Rotator Cuff/pathology , Rotator Cuff/surgery , Shoulder Impingement Syndrome/surgery , Treatment Outcome
12.
Einstein (Sao Paulo) ; 12(3): 351-4, 2014 Sep.
Article in English, Portuguese | MEDLINE | ID: mdl-25167335

ABSTRACT

The impingement syndrome is defined by the compression of the rotator cuff tendons against the coracoacromial arch. Several factors contribute to this condition and they are classified as structural or functional factors. The former are changes in the coracoacromial arch, proximal humerus, bursa and rotator cuff, and the latter are related to the mechanism of the upper limb by means of synchronized activity and balanced between the rotator cuff and scapular girdle muscles. The authors report here a case of parosteal lipoma of the proximal humerus, located between the muscles deltoid, teres minor and infraspinatus causing clinical signs of impingement. It is a rare occurrence, characterized as a structural cause for the onset of this symptom.


Subject(s)
Deltoid Muscle , Lipoma/complications , Muscle Neoplasms/complications , Shoulder Impingement Syndrome/etiology , Aged, 80 and over , Deltoid Muscle/pathology , Deltoid Muscle/surgery , Female , Humans , Lipoma/pathology , Lipoma/surgery , Magnetic Resonance Imaging , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery , Rotator Cuff/pathology , Rotator Cuff/surgery , Shoulder Impingement Syndrome/surgery , Treatment Outcome
13.
Arq Bras Endocrinol Metabol ; 57(4): 317-21, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23828437

ABSTRACT

Distant metastases of differentiated thyroid cancer are unusual; lung and bones are the most frequently affected sites. Soft tissue metastases (STM) are extremely rare. We describe two cases of patients with differentiated thyroid cancer metastasizing to soft tissues. Both patients had widespread metastatic disease; clinically asymptomatic soft tissue metastases were found by ¹8-Fluordeoxyglucose positron emission tomography/computed tomography (¹8F FDG PET-CT), and confirmed by cytological and/or histopathological studies. These findings underscore the ability of ¹8F FDG PET-CT in accurately assessing the extent of the disease, as well as the utility of the method to evaluate regions of the body that are not routinely explored.


Subject(s)
Fluorodeoxyglucose F18 , Multimodal Imaging/methods , Radiopharmaceuticals , Soft Tissue Neoplasms/secondary , Thyroid Neoplasms/pathology , Adenocarcinoma, Papillary/pathology , Adult , Biopsy, Fine-Needle , Female , Humans , Male , Middle Aged , Muscle Neoplasms/pathology , Muscle Neoplasms/secondary , Neoplasm Metastasis , Positron-Emission Tomography/methods , Skin Neoplasms/secondary , Tomography, X-Ray Computed/methods
14.
Arq. bras. endocrinol. metab ; Arq. bras. endocrinol. metab;57(4): 317-321, June 2013. ilus
Article in English | LILACS | ID: lil-678147

ABSTRACT

Distant metastases of differentiated thyroid cancer are unusual; lung and bones are the most frequently affected sites. Soft tissue metastases (STM) are extremely rare. We describe two cases of patients with differentiated thyroid cancer metastasizing to soft tissues. Both patients had widespread metastatic disease; clinically asymptomatic soft tissue metastases were found by 18-Fluordeoxyglucose positron emission tomography/computed tomography (18F FDG PET-CT), and confirmed by cytological and/or histopathological studies. These findings underscore the ability of 18F FDG PET-CT in accurately assessing the extent of the disease, as well as the utility of the method to evaluate regions of the body that are not routinely explored.


As metástases a distância em carcinoma diferenciado de tireoide são raras. Pulmão e ossos são os lugares mais frequentemente atingidos. As metástases em tecidos moles são extremamente infrequentes. Neste artigo, descrevemos dois casos de pacientes com câncer diferenciado de tireoide com metástases em tecidos moles. Ambos os pacientes padeciam de enfermidade avançada. As metástases em partes moles foram assintomáticas e detectadas mediante 18-Fluordeoxyglucose positron emission tomography/computed tomography (18F FDG PET-CT), sendo confirmadas por citologia e/ou histopatologia. Esses achados ressaltam o valor do 18F FDG PET-CT para a avaliação correta da extensão da enfermidade e a utilidade do método para avaliar regiões do corpo que não são exploradas nos estudos de rotina.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Multimodal Imaging/methods , Radiopharmaceuticals , Soft Tissue Neoplasms/secondary , Thyroid Neoplasms/pathology , Adenocarcinoma, Papillary/pathology , Biopsy, Fine-Needle , Muscle Neoplasms/pathology , Muscle Neoplasms/secondary , Neoplasm Metastasis , Positron-Emission Tomography/methods , Skin Neoplasms/secondary , Tomography, X-Ray Computed/methods
15.
An Bras Dermatol ; 86(5): 1029, 2011.
Article in English, Portuguese | MEDLINE | ID: mdl-22147052

ABSTRACT

Glomus tumor is a painful tumor derived from the glomus terminal which regulates blood circulation and body temperature Despite its rarity, particular attention needs to be paid to symptoms associated with this tumor: paroxysmal pain, sensitivity to local pressure and cold, and its location - typically in the distal phalanx. Manifestation of extradigital occurrence is possible. Single lesions are most common in adult females, while multiple lesions are prevalent in children and adolescents, generally those with a positive family history. The diagnosis is clinical with the aid of ultrasonography and magnetic resonance imaging, confirmed by histopathological examination.


Subject(s)
Foot/pathology , Glomus Tumor/pathology , Muscle Neoplasms/pathology , Adult , Diagnosis, Differential , Humans , Male
17.
Article in English | MEDLINE | ID: mdl-20303057

ABSTRACT

Alveolar soft-part sarcoma (ASPS) is a rare malignant neoplasm with uncertain histogenesis and with a distinctive morphology. It has been described in the oral cavity, but this is the first report of ASPS metastasizing to the maxillary tuber region. A 27-year-old male patient, who was under chemotherapy treatment for ASPS of the thigh, presented in our dental clinic with a painless and pedunculated nodule on the right tuber maxillae. The nodule was erythematous with smooth and lobular surface, measuring 3 cm in maximum diameter. An incisional biopsy was performed and the diagnosis of metastatic ASPS was made. Histologically, the tumor was characterized by a proliferation of polyhedral cells in pseudoalveolar pattern. Tumor cells were large, showing granular cytoplasm, periodic acid-Schiff positive diastase-resistant intracytoplasmic material, and vesicular nuclei with prominent nucleoli. Unfortunately, the patient died 2 months after the diagnosis of the oral metastasis. Metastases of ASPS to the mouth are very rare and indicate a poor prognosis.


Subject(s)
Gingival Neoplasms/secondary , Maxilla/pathology , Sarcoma, Alveolar Soft Part/secondary , Adult , Brain Neoplasms/secondary , Cell Nucleolus/ultrastructure , Cell Nucleus/ultrastructure , Cytoplasm/ultrastructure , Diagnosis, Differential , Fatal Outcome , Gingival Diseases/diagnosis , Granuloma, Giant Cell/diagnosis , Granuloma, Pyogenic/diagnosis , Humans , Male , Muscle Neoplasms/pathology , Sarcoma, Alveolar Soft Part/pathology , Thigh/pathology
18.
Int J Dermatol ; 48(8): 875-8, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19659867

ABSTRACT

BACKGROUND: Hemangiomas are benign endothelial cell-derived tumors that are present in 1-2% of newborns. They are most frequent in females. Eighty per cent are located in the head and neck region. Intramuscular hemangiomas represent 0.8% of all cases. They are characterized by rapid endothelial growth. Treatment is indicated for lesions that have an organic or visceral location or those that present with deformities. METHODS: Six cases of intramuscular hemangioma are presented. They were collected during the period June 2003 to November 2005 from all surgical cases seen at the Department of Cardiovascular Surgery, Hospital General "Dr Manuel Gea Gonzalez," Mexico City, Mexico. Their clinical appearance, treatment, and outcomes are discussed. RESULTS: There were five women and one man with a mean age of 24.6 years (15-44 years). Two hemangiomas were located on the upper extremities and four on the lower extremities. All six patients were treated by surgical resection. Four cavernous hemangiomas were revealed during microscopic examination. At 1-3 years of follow-up, there were no recurrences and the functional and aesthetic results were good. CONCLUSIONS: Intramuscular hemangiomas are rare. Lesions of the extremities are even rarer. Surgical excision in the six cases described here resulted in cure with good functional and cosmetic outcomes.


Subject(s)
Hemangioma/pathology , Hemangioma/surgery , Magnetic Resonance Imaging , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery , Adolescent , Adult , Buttocks , Female , Forearm , Hand , Humans , Knee , Male , Surgery, Plastic , Thigh , Young Adult
19.
Eur Spine J ; 18 Suppl 2: 245-9, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19301043

ABSTRACT

Myxoma is a neoplasm of mesenchymal origin composed of undifferentiated stellate cells in a myxoid stroma. This tumor can develop in a variety of locations. Myxomas that arise from skeletal muscles are called intramuscular myxomas. They usually occur in large skeletal muscles. Only ten cases of these benign tumors involving the neck muscles were reported in literature. Of them, only three were located at the paraspinal muscles. A 64-year-old woman presented with occipital and neck pain over 5 years noted an expansive painful lesion located at posterior cervical region with progressive volume increase in the last 12 months. Image exams revealed a large mass located in the left posterior region of the neck in contact with the C2, C3 and C4 laminae with no invasion of the vertebrae. Tumor total removal was performed through normal muscle margins and the vertebral periosteum was scraped. The tumor was encapsulated, lobulated with a gray-white appearance. The histological examination yielded the diagnosis of intramuscular myxoma. Follow-up at 1 year showed complete resolution of preoperative symptoms and no evidence of local recurrence. In conclusion, although rare, intramuscular myxoma should be included in differential diagnosis of cervical paraspinal tumors. We reported the fourth case of intramuscular myxoma in the paraspinal musculature of the neck. Despite its benign characteristics, local recurrence was reported after subtotal resection. Tumor total removal should be the goal of surgery.


Subject(s)
Cervical Vertebrae , Muscle Neoplasms/diagnosis , Muscle, Skeletal , Myxoma/diagnosis , Cervical Vertebrae/diagnostic imaging , Cervical Vertebrae/pathology , Diagnosis, Differential , Female , Humans , Magnetic Resonance Imaging , Middle Aged , Muscle Neoplasms/pathology , Muscle Neoplasms/surgery , Muscle, Skeletal/diagnostic imaging , Muscle, Skeletal/pathology , Myxoma/pathology , Myxoma/surgery , Tomography, X-Ray Computed , Treatment Outcome
20.
Rev Med Chil ; 132(8): 985-8, 2004 Aug.
Article in Spanish | MEDLINE | ID: mdl-15478301

ABSTRACT

We report a 67 years old male with a history of pulmonary tuberculosis at the age of 15, that consults for malaise, weight loss and productive cough. Chest X ray examination showed a left pleural effusion. A pleural tap obtained a sterile exudate. A thorax CAT scan showed a proliferating mass in the splenic angle of the colon, with left lung and diaphragmatic invasion. Endoscopic biopsies confirmed the diagnosis of adenocarcinoma. The patient underwent a subtotal colectomy with partial excision of diaphragm and left lung. The pathological report showed a mucosecretory adenocarcinoma, infiltrating the pericolonic adipose tissue without adjacent organ infiltration and a chronic inflammatory process involving colonic serosa, diaphragm pleura, and lung. Adjuvant chemotherapy was indicated and the patient is asymptomatic and without evidences of tumor recurrence after a 24 months follow up.


Subject(s)
Adenocarcinoma, Mucinous , Colorectal Neoplasms , Diaphragm , Lung Neoplasms , Muscle Neoplasms/pathology , Adenocarcinoma, Mucinous/pathology , Adenocarcinoma, Mucinous/surgery , Aged , Colorectal Neoplasms/pathology , Colorectal Neoplasms/surgery , Diaphragm/pathology , Diaphragm/surgery , Follow-Up Studies , Humans , Lung Neoplasms/pathology , Lung Neoplasms/surgery , Male , Muscle Neoplasms/surgery , Neoplasm Invasiveness
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