Pulmonary alveolar microlithiasis with involvement of the sympathetic nervous system and gonads.

نویسنده

  • T Coetzee
چکیده

Pulmonary alveolar microlithiasis is a relatively rare disease, of obscure aetiology, manifested by the presence of intra-alveolar laminated concretions distributed diffusely throughout the lungs. In all the recorded cases disease has been limited to the lungs and similar lesions have not been observed in other organs or tissues. The findings in a patient in whom lesions identical to those in the lungs were confirmed in the lumbar sympathetic chain and suspected to be present in the testes are recorded. The patient, an African man aged 24 years from the Griqualand East area of South Africa, came under medical care in October 1963 when he presented with an attack of acute abdominal pain. No diagnosis was made. He had a similar attack three months later. Examination was largely negative. Radiographs of the pelvis showed scattered lines of calcification, not characteristic of that occurring in bilharzial involvement of the bladder. Laparotomy revealed no gross abnormalities. Because the possibility of a recurring pancreatitis could not be excluded, a sphincterotomy was performed. He was seen by the author four months later, during an attack of abdominal pain associated with diarrhoea , vomiting, and urinary difficulty. He responded slowly to conservative treatment and it was decided to undertake further special examinations in an attempt to establish a diagnosis. Special interrogation revealed that the patient had three brothers and three sisters. One sister had died at 23 years of age of a lung disease, but no details were available. Two brothers were available for medical examination: they were both in good health and chest radiographs were normal. There was no history of taking snuff or chewing tobacco. He smoked and drank beer in moderation. There was no opportunity for close contact with bats. The patient appeared thin but was otherwise in good physical condition. There were no significant findings on general examination apart from slight hyperextensibility of the finger joints. Clinical examination of the respiratory, cardiovascular, and nervous systems revealed no abnormalities. The abdomen showed normal findings on examination. The chest radiograph showed miliary opacities scattered throughout both lungs (Fig. 1). Repeated sputum examinations were negative for tuberculosis and showed no malignant cells. An intravenous pyelo-gram showed normal renal excretion and anatomy and a normal cystogram with good bladder evacuation. The urine was normal on chemical and microscopic examination. The linear opacities previously noted were seen in the pelvis, and a linear opacity could also be …

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Microlithiasis of Seminal Vesicles and Severe Oligoasthenospermia in Pulmonary Alveolar Microlithiasis (PAM): Report of An Unusual Sporadic Case

s:696:"Pulmonary alveolar microlithiasis (PAM) is classified as an elective dysmetabolic thesaurotic pneumoalveolitis and characterized by the presence within the alveoli of the lungs of myriad of tiny calculi. The classic presentation of the chest radiography is unmistakable with multiple small "sand-like" opacities diffusely involving both lung fields. We present a case of male infertility fo...

متن کامل

A Case Report of Pulmonary Alveolar Microlithiasis

Pulmonary alveolar microlithiasis is a rare autosomal recessive disease characterized by the formation of calcium phosphate deposition in the alveoli. Although the disease most often occurs in children, most patients with the disease are diagnosed in adulthood due to the slow progression of the disease inside the lungs. In childhood, it often causes no symptoms, and changes in the lung parenchy...

متن کامل

Pulmonary Alveolar Microlithiasis: A Rare Case Report

Pulmonary alveolar microlithiasis is an uncommon infiltrative pulmonary disease characterized by deposition of microliths in the alveoli. We present the case of a young adult with complaints of shortness of breath on exertion. Chest radiograph showed innumerable small, dense nodules, diffusely involving both the lungs - predominantly in the lower zones. High-resolution CT scan illustrated wides...

متن کامل

Pulmonary alveolar microlithiasis with homozygous c.316G > C (p.G106R) mutation: a case report.

Pulmonary alveolar microlithiasis is characterized by the presence of calcospherites in alveolar spaces. Sporadic cases are more common, but the disease also presents in an inherited familial form. The greatest number of reported cases is from Europe and especially Turkey. We present a 43-year-old female with complaints of dyspnea for many years. She had a suspicious familial ...

متن کامل

بیماری میکرولیتیاز آلوئولی همراه با استئوپتروز

  Background : Pulmonary alveolar microlithiasis is a rare condition characterized by a diffuse bilateral filling of the majority of alveoli by calcific concretions called calcospherits. The etiology and pathogenesis are obscure. Osteopetrosis is a heterogenous group of heritable conditions with defect in bone resorption by osteoclasts. Materials & Methods: We report a case of pulmonary alveola...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Thorax

دوره 25 5  شماره 

صفحات  -

تاریخ انتشار 1970