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1.
Diagnosis (Berl) ; 11(2): 212-217, 2024 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-38387019

RESUMEN

OBJECTIVES: Lung cancer is the leading cause of cancer-related death and poses significant challenges in diagnosis and management. Although muscle metastases are exceedingly rare and typically not the initial clinical manifestation of neoplastic processes, their recognition is crucial for optimal patient care. CASE PRESENTATION: We present a case report in which we identify the unique scenario of a 60-year-old man with shoulder pain and a deltoid muscle mass, initially suggestive of an undifferentiated pleomorphic sarcoma. However, further investigations, including radiological findings and muscle biopsy, revealed an unexpected primary lung adenocarcinoma. We performed a systematic literature search to identify the incidence of SMM and reflect on how to improve and build on better diagnosis for entities as atypical as this. This atypical presentation highlights the importance of recognizing and addressing cognitive biases in clinical decision-making, as acknowledging the possibility of uncommon presentations is vital. By embracing a comprehensive approach that combines imaging studies with histopathological confirmation, healthcare providers can ensure accurate prognoses and appropriate management strategies, ultimately improving patient outcomes. CONCLUSIONS: This case serves as a reminder of the need to remain vigilant, open-minded, and aware of cognitive biases when confronted with uncommon clinical presentations, emphasizing the significance of early recognition and prompt evaluation in achieving optimal patient care.


Asunto(s)
Neoplasias Pulmonares , Dolor de Hombro , Humanos , Masculino , Dolor de Hombro/etiología , Dolor de Hombro/diagnóstico , Persona de Mediana Edad , Neoplasias Pulmonares/diagnóstico , Neoplasias Pulmonares/complicaciones , Razonamiento Clínico , Diagnóstico Diferencial , Adenocarcinoma del Pulmón/diagnóstico , Adenocarcinoma del Pulmón/patología , Adenocarcinoma del Pulmón/complicaciones , Sarcoma/diagnóstico , Toma de Decisiones Clínicas , Músculo Deltoides/patología , Tomografía Computarizada por Rayos X , Biopsia
4.
Arch Orthop Trauma Surg ; 141(7): 1149-1154, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-32529387

RESUMEN

INTRODUCTION: Reverse shoulder arthroplasty (RSA) shows promising short- and mid-term results in cuff tear arthropathy. However, functional impairments are described in long-term findings. Micromorphological changes in the periarticular musculature could be in part responsible for this, but have not yet been analysed. Thus, histological changes of the deltoid muscle and their association to the functional outcome were evaluated in this study. MATERIAL AND METHODS: A total of 15 patients treated with RSA were included in this prospective study. Functional outcome was assessed using the Constant Score (CS) and the DASH (disabilities of the arm, shoulder and hand) Score before RSA and after a mean follow-up of 12 months. Deltoid muscle biopsies were harvested intraoperatively and 12 months postoperatively. Mean deltoid muscle fibre area (MMFA) was calculated histologically after haematoxylin-eosin staining. RESULTS: Postoperative shoulder function significantly improved within 12 months (CS: Δ 37.4 ± 22.6, p = 0.001; DASH: Δ 27.1 ± 29.1, p = 0.006). The MMFA significantly decreased (p = 0.02), comparing the results from the intraoperative biopsy (MMFA: 8435.8 µm2, SD ± 5995.9 µm2) to the 12 months biopsy (MMFA: 5792. µm2, SD ± 3223.6 µm2). No correlation could be found between the functional score results and MMFA. CONCLUSION: Signs of deltoid muscle changes in terms of a reduced MMFA can be detected 1 year after RSA and thus already a long time before long-term functional impairments become apparent. Further studies with larger patient series and longer follow-up periods as well as extended histological assessments and simultaneous radiological examinations are required.


Asunto(s)
Artroplastía de Reemplazo de Hombro , Músculo Deltoides , Articulación del Hombro/cirugía , Artroplastía de Reemplazo de Hombro/efectos adversos , Artroplastía de Reemplazo de Hombro/métodos , Músculo Deltoides/patología , Músculo Deltoides/cirugía , Humanos , Estudios Prospectivos
5.
Genes (Basel) ; 11(12)2020 12 19.
Artículo en Inglés | MEDLINE | ID: mdl-33352713

RESUMEN

Primary mitochondrial myopathies (PMM) are a group of mitochondrial disorders characterized by a predominant skeletal muscle involvement. The aim of this study was to evaluate whether the biochemical profile determined by Fourier-transform infrared (FTIR) spectroscopic technique would allow to distinguish among patients affected by progressive external ophthalmoplegia (PEO), the most common PMM presentation, oculopharyngeal muscular dystrophy (OPMD), and healthy controls. Thirty-four participants were enrolled in the study. FTIR spectroscopy was found to be a sensitive and specific diagnostic marker for PEO. In particular, FTIR spectroscopy was able to distinguish PEO patients from those affected by OPMD, even in the presence of histological findings similar to mitochondrial myopathy. At the same time, FTIR spectroscopy differentiated single mtDNA deletion and mutations in POLG, the most common nuclear gene associated with mitochondrial diseases, with high sensitivity and specificity. In conclusion, our data suggest that FTIR spectroscopy is a valuable biodiagnostic tool for the differential diagnosis of PEO with a high ability to also distinguish between single mtDNA deletion and mutations in POLG gene based on specific metabolic transitions.


Asunto(s)
ADN Mitocondrial/genética , Músculo Deltoides/química , Miopatías Mitocondriales/diagnóstico , Espectroscopía Infrarroja por Transformada de Fourier , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Biopsia , Niño , ADN Polimerasa gamma/genética , ADN Mitocondrial/análisis , Músculo Deltoides/patología , Diagnóstico Diferencial , Femenino , Humanos , Masculino , Persona de Mediana Edad , Miopatías Mitocondriales/genética , Miopatías Mitocondriales/patología , Distrofia Muscular Oculofaríngea/diagnóstico , Distrofia Muscular Oculofaríngea/patología , Oftalmoplejía Externa Progresiva Crónica/diagnóstico , Oftalmoplejía Externa Progresiva Crónica/patología , Sensibilidad y Especificidad , Adulto Joven
6.
JBJS Case Connect ; 10(1): e0210, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32224643

RESUMEN

CASE: A 34-year-old man with poorly controlled acquired immune deficiency syndrome underwent excision of a left arm mass. The histopathologic workup identified the features of an Epstein-Barr virus-associated smooth muscle tumor (EBV-SMT). The patient was readmitted 5 months later for vomiting and found to have liver metastases that were confirmed to be EBV-SMT. Six months after discharge, there was no recurrence of the arm mass or increase in the size of the liver metastases. CONCLUSION: Most commonly found in immunocompromised patients, EBV-SMTs are rare tumors that can be mistaken for a leiomyosarcoma.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/complicaciones , Músculo Deltoides/patología , Infecciones por Virus de Epstein-Barr/complicaciones , Herpesvirus Humano 4/aislamiento & purificación , Tumor de Músculo Liso/virología , Neoplasias de los Tejidos Blandos/virología , Adulto , Humanos , Masculino , Tumor de Músculo Liso/diagnóstico por imagen , Tumor de Músculo Liso/patología , Tumor de Músculo Liso/cirugía , Neoplasias de los Tejidos Blandos/diagnóstico por imagen , Neoplasias de los Tejidos Blandos/patología , Neoplasias de los Tejidos Blandos/cirugía
7.
Jpn J Clin Oncol ; 50(7): 772-778, 2020 Jul 09.
Artículo en Inglés | MEDLINE | ID: mdl-32249309

RESUMEN

BACKGROUND: The present study aimed to determine functional outcomes in patients undergoing deltoid muscle resection for soft tissue sarcoma. METHODS: Between 2002 and 2014, 18 patients with soft tissue sarcoma of the shoulder who underwent wide resection including the deltoid muscle, and were followed up for more than 12 months, were retrospectively included in the study. In all, 11 patients were male and 7 were female. The median age was 59 years, median follow-up duration was 37 months. The extent of resection of deltoid muscle, with or without rotator cuff damage, reconstruction methods, adjuvant therapy, oncological outcomes, and the International Society of Limb Salvage (ISOLS) score as functional outcomes were analyzed. RESULTS: Six patients underwent total resection, and twelve underwent partial resections of deltoid muscle. The rotator cuff was resected in four patients. Soft tissue reconstruction was performed in 17 patients using a pedicled latissimus dorsi muscle flap. Two local recurrences and three distant metastases occurred during follow-up. Median overall survival was 72 months. The mean ISOLS score was 25.0 points (±4.6points). Univariate analysis revealed that there was no significant difference in ISOLS score regarding the extent of deltoid muscle resection. Multivariate analysis identified only combined resection of the rotator cuff as a significant prognostic factor for poor functional outcomes (P < 0.001). CONCLUSIONS: The extent of resection of the deltoid muscle might not affect the functional outcomes determined by ISOLS score. If the rotator cuff is resected concurrently, satisfactory functional outcomes might not be obtained.


Asunto(s)
Músculo Deltoides/cirugía , Neoplasias de los Tejidos Blandos/complicaciones , Músculo Deltoides/patología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Neoplasias de los Tejidos Blandos/patología , Resultado del Tratamiento
8.
Ann Clin Transl Neurol ; 7(5): 846-854, 2020 05.
Artículo en Inglés | MEDLINE | ID: mdl-32307885

RESUMEN

Congenital titinopathies are myopathies with variable phenotypes and inheritance modes. Here, we fully characterized, using an integrated approach (deep phenotyping, muscle morphology, mRNA and protein evaluation in muscle biopsies), two siblings with congenital multicore myopathy harboring three TTN variants predicted to affect titin stability and titin-myosin interactions. Muscle biopsies showed multicores, type 1 fiber uniformity and sarcomeric structure disruption with some thick filament loss. Immunohistochemistry and Western blotting revealed a marked reduction of fast myosin heavy chain isoforms. This is the first observation of a titinopathy suggesting that titin defect leads to secondary loss of fast myosin heavy chain isoforms.


Asunto(s)
Conectina/genética , Enfermedades Musculares , Cadenas Pesadas de Miosina/deficiencia , Adolescente , Niño , Músculo Deltoides/patología , Femenino , Humanos , Masculino , Enfermedades Musculares/congénito , Enfermedades Musculares/genética , Enfermedades Musculares/metabolismo , Enfermedades Musculares/patología , Linaje , Hermanos
9.
Muscle Nerve ; 61(3): 390-395, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-31820462

RESUMEN

INTRODUCTION: After traumatic nerve injury, neuromuscular junction remodeling plays a key role in determining functional outcomes. Immunohistochemical analyses of denervated muscle biopsies may provide valuable prognostic data regarding clinical outcomes to supplement electrodiagnostic studies. METHODS: We performed biopsies on nonfunctioning deltoid muscles in two patients after gunshot wounds and visualized the neuromuscular junctions using two-photon microscopy with immunohistochemistry. RESULTS: Although the nerves in both patients showed evidence of acute Wallerian degeneration, some of the motor endplates were intact but exhibited significantly decreased surface area and volume. Both patients exhibited substantial recovery of motor function over several weeks postinjury. DISCUSSION: Two-photon microscopic assessment of neuromuscular junction integrity and motor endplate morphometry in muscle biopsies provided evidence of partial sparing of muscle innervation. This finding supported the clinical judgment that eventual recovery would occur. With further study, this technique may help to guide operative decisionmaking after traumatic nerve injuries.


Asunto(s)
Neuropatías del Plexo Braquial/diagnóstico , Neuropatías del Plexo Braquial/patología , Placa Motora/patología , Adulto , Neuropatías del Plexo Braquial/fisiopatología , Músculo Deltoides/inervación , Músculo Deltoides/patología , Electromiografía , Humanos , Masculino , Microscopía , Placa Motora/fisiología , Conducción Nerviosa , Imagen Óptica , Adulto Joven
10.
Neuromuscul Disord ; 29(9): 678-683, 2019 09.
Artículo en Inglés | MEDLINE | ID: mdl-31474437

RESUMEN

Emery-Dreifuss muscular dystrophy is an early-onset, slowly progressive myopathy characterized by the development of multiple contractures, muscle weakness and cardiac dysfunction. We present here the case of a 65-year-old male patient with a 20 year history of slowly progressive camptocormia, bradycardia and shortness of breath. Examination showed severe spine extensor and neck flexor muscle weakness with slight upper limb proximal weakness. Cardiologic assessment revealed slow atrial fibrillation. Whole body MRI demonstrated adipose substitution of the paravertebral, limb girdle and peroneal muscles as well as the tongue. Emerin immunohistochemistry on patient muscle biopsy revealed the absence of nuclear envelope labeling confirmed by Western Blot. Genetic analysis showed a hemizygous duplication of 5 bases in exon 6 of the EMD, emerin, gene on the X chromosome. This is an unusual presentation of X-linked Emery-Dreifuss muscular dystrophy with adult onset, predominant axial muscles involvement and minimal joint contractures. Diagnosis was prompted by the analysis of emerin on muscle biopsy.


Asunto(s)
Proteínas de la Membrana/genética , Músculo Esquelético/diagnóstico por imagen , Distrofia Muscular de Emery-Dreifuss/genética , Proteínas Nucleares/genética , Edad de Inicio , Anciano , Fibrilación Atrial/fisiopatología , Músculos de la Espalda/diagnóstico por imagen , Bradicardia/fisiopatología , Contractura/fisiopatología , Músculo Deltoides/metabolismo , Músculo Deltoides/patología , Disnea/fisiopatología , Músculos Isquiosurales/diagnóstico por imagen , Humanos , Imagen por Resonancia Magnética , Masculino , Músculos Masticadores/diagnóstico por imagen , Proteínas de la Membrana/metabolismo , Músculo Esquelético/metabolismo , Músculo Esquelético/patología , Atrofia Muscular Espinal/fisiopatología , Distrofia Muscular de Emery-Dreifuss/diagnóstico por imagen , Distrofia Muscular de Emery-Dreifuss/patología , Distrofia Muscular de Emery-Dreifuss/fisiopatología , Proteínas Nucleares/metabolismo , Índice de Severidad de la Enfermedad , Curvaturas de la Columna Vertebral/fisiopatología
13.
Skeletal Radiol ; 48(4): 625-628, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30187111

RESUMEN

Leiomyomas are benign tumors of smooth muscle cells. Leiomyomas of somatic soft tissue are a specific class of leiomyoma believed to arise from the smooth muscle cells found in the walls of blood vessels and represent less than 4% of benign, somatic soft tissue tumors. Of the somatic soft tissue tumors, approximately one-third will become calcified. We report an intramuscular, calcified leiomyoma arising from the left deltoid of a 47-year-old Caucasian male. To the best of the authors' knowledge, this is the first reported case of a calcified, intramuscular leiomyoma of the deltoid. Imaging studies and patient presentation were initially suggestive of tumoral calcinosis or myositis ossificans. It was not until pathologic examination that the correct diagnosis of the calcified leiomyoma was made. Leiomyoma should be included in the differential diagnosis of calcified soft tissue masses. If excised with adequate margins, recurrence is unlikely.


Asunto(s)
Calcinosis/diagnóstico por imagen , Músculo Deltoides/diagnóstico por imagen , Leiomioma/diagnóstico por imagen , Calcinosis/patología , Calcinosis/cirugía , Medios de Contraste , Músculo Deltoides/patología , Músculo Deltoides/cirugía , Diagnóstico Diferencial , Humanos , Leiomioma/patología , Leiomioma/cirugía , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad
16.
Clín. investig. ginecol. obstet. (Ed. impr.) ; 44(3): 134-135, jul.-sept. 2017.
Artículo en Español | IBECS | ID: ibc-164934

RESUMEN

Las metástasis intramusculares son un hallazgo muy infrecuente, suponen aproximadamente el 1% de las metástasis, siendo más frecuente a nivel de musculatura abdominal y miembros inferiores. Esta baja incidencia es debido a que existen diferentes mecanismos de resistencia al desarrollo de las mismas, además existe un infradiagnóstico de las mismas por su baja sintomatología


Intramuscular metastases are rarely diagnosed, it about 1% all kind of metastases, and frequently are localized in the abdominal muscles and lower extremity. Low incidence is due to different resistance mechanisms to its develop, thus an underdiagnosis because its low symptomatology


Asunto(s)
Humanos , Femenino , Anciano , Músculo Deltoides/patología , Neoplasias de los Músculos/secundario , Neoplasias Ováricas/patología , Metástasis de la Neoplasia/patología , Carcinoma Papilar/patología
18.
In Vivo ; 31(4): 657-660, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28652434

RESUMEN

BACKGROUND/AIM: To investigate the contribution of muscle tissue-derived cytokines in dermatomyositis (DM). MATERIALS AND METHODS: Muscle homogenates were prepared from deltoid muscle biopsy specimens of 10 patients with DM and eight controls with no pathological signs of myopathy. Interleukin (IL)-4, interferon (IFN)-γ and IL-17 levels were evaluated by enzyme-linked immunosorbent assay (ELISA) and immunoblotting analysis. Muscle strength grades were recorded. RESULTS: Patients with DM showed significantly elevated muscle tissue IL-4 and IFN-γ levels, whereas IL-17 levels were comparable between patients with DM and controls. Immunoblotting studies confirmed ELISA results. In DM muscle specimens, IL-4 and IFN-γ levels were positively correlated, while no correlation was observed between IL-17 and the other two cytokines. Moreover, IL-4 and IFN-γ levels were significantly negative correlated with muscle strength grades for the deltoid muscle. CONCLUSION: Our results confirm the involvement of T helper (Th) 1-type and Th2-type immunity in DM pathogenesis. Muscle tissue appears to contribute to muscle weakness in DM by producing inflammatory cytokines.


Asunto(s)
Dermatomiositis/genética , Interferón gamma/genética , Interleucina-17/genética , Interleucina-4/genética , Adulto , Anciano , Biopsia , Músculo Deltoides/metabolismo , Músculo Deltoides/patología , Dermatomiositis/patología , Ensayo de Inmunoadsorción Enzimática , Femenino , Regulación de la Expresión Génica , Humanos , Inflamación/genética , Inflamación/patología , Masculino , Persona de Mediana Edad , Músculos/metabolismo , Músculos/patología
19.
PLoS One ; 12(3): e0174361, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28355234

RESUMEN

We aimed to estimate the interrelation between preoperative deltoid muscle status by measuring the 3-dimensional deltoid muscle volume and postoperative functional outcomes after reverse total shoulder arthroplasty(RTSA). Thirty-five patients who underwent RTSA participated in this study. All patients underwent preoperative magnetic resonance imaging(MRI) as well as pre- and postoperative radiography and various functional outcome evaluations at least 1 year. The primary outcome parameter was set as age- and sex-matched Constant scores. The 3-dimensional deltoid muscle model was generated using a medical image processing software and in-house code, and the deltoid muscle volume was calculated automatically. Various clinical and radiographic factors comprising the deltoid muscle volume adjusted for body mass index(BMI) were analyzed, and their interrelation with the outcome parameters was appraised using a multivariate analysis. As a result, all practical consequences considerably improved following surgery(all p<0.01). Overall, 20 and 15 indicated a higher and a lower practical consequence than the average, respectively, which was assessed by the matched Constant scores. The deltoid muscle volume adjusted for BMI(p = 0.009), absence of a subscapularis complete tear (p = 0.040), and greater change in acromion-deltoid tuberosity distance(p = 0.013) were associated with higher matched Constant scores. Multivariate analysis indicated that the deltoid muscle volume was the single independent prognostic factor for practical consequences(p = 0.011). In conclusion, the preoperative deltoid muscle volume significantly affected the functional outcome following RTSA in patients with cuff tear arthropathy or irreparable cuff tears. Therefore, more attention should be paid to patients with severe atrophied deltoid muscle who are at a high risk for poor practical consequences subsequent to RTSA.


Asunto(s)
Artroplastía de Reemplazo de Hombro , Músculo Deltoides/patología , Artropatía por Desgarro del Manguito de los Rotadores/cirugía , Anciano , Anciano de 80 o más Años , Músculo Deltoides/diagnóstico por imagen , Músculo Deltoides/fisiopatología , Femenino , Humanos , Masculino , Contracción Muscular , Tamaño de los Órganos , Rango del Movimiento Articular , Recuperación de la Función , Artropatía por Desgarro del Manguito de los Rotadores/diagnóstico por imagen , Articulación del Hombro/diagnóstico por imagen , Articulación del Hombro/fisiopatología , Articulación del Hombro/cirugía , Resultado del Tratamiento
20.
J Med Case Rep ; 11(1): 13, 2017 Jan 14.
Artículo en Inglés | MEDLINE | ID: mdl-28086945

RESUMEN

BACKGROUND: Musculoskeletal tumors involving the deltoid muscle and necessitating its complete resection are rare. The function after complete deltoid resection is reported to be limited, and several authors consider muscle transfer to improve shoulder motion. However, it still remains unclear whether such transfer adds function. To the best of our knowledge, all reports on complete deltoid resection refer to adult patients, and it is unknown what function results after deltoid resection in childhood. The remaining muscles may have the potential to compensate for the loss of deltoid function. CASE PRESENTATION: Here we report the case of a 5-year-old white boy with complete (isolated) deltoid muscle resection in infancy for a large aggressive soft tissue tumor. No reconstructive procedure or muscle transfer was performed at the time of index surgery. Pathology revealed an angiomatoid fibrous histiocytoma. His postoperative course was uneventful. At 11 years of follow-up, he remained disease-free and had excellent shoulder function, including normal range of motion. CONCLUSIONS: This report implies that major muscles such as the deltoid can be resected in a child without compromising long-term function. Therefore, a muscle transfer at index surgery is probably not necessary.


Asunto(s)
Músculo Deltoides/patología , Histiocitoma Fibroso Maligno/cirugía , Procedimientos de Cirugía Plástica/métodos , Articulación del Hombro/patología , Neoplasias de los Tejidos Blandos/cirugía , Preescolar , Músculo Deltoides/cirugía , Estudios de Seguimiento , Histiocitoma Fibroso Maligno/patología , Humanos , Masculino , Rango del Movimiento Articular , Neoplasias de los Tejidos Blandos/patología , Resultado del Tratamiento
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