case report case of superior longitudinal sinus … · sinus and thence to the left jugular vein...

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POSTGRAD. MED. J. (1965), 41, 702. SUPERIOR LONGITUDINAL SINUS THROMBOSIS IN PREGNANCY D. J. RICHARDS, B.Sc., M.B., Ch.B., M.R.C.S., L.R.C.P.* Registrar in General Medicine, Hallam Hospital, West Bromwich. PRIMARY (aseptic, marasmic or autochthonous) thrombosis of the superior sagittal sinus, that is where local inflammation plays no part (Bertier, 1907), is an uncommon condition. It was first noted that the puerperium could predispose to its formation by Gowers (1888), but description of cases occurring during preg- nancy itself are rare. Case Report Mrs. B.M., aged 29 years, was admitted on the 29th April, 1964, to Hallam Hospital, West Brom- wich. She was 12 weeks pregnant and had been vomiting fairly consistently for eight weeks. The general practitioner had diagnosed this as hyper- emesis gravidarum and had treated her with pro- chlorperazine (Stemetil). On the day of admission she was found in bed having a generalised fit with tongue biting and incontinence. There was no history of epileptic convulsions in the family. The previous three pregnancies in 1956, 58 and 62 were uneventful apart from a post-partum haemorrhage with the first. The relatives stated that two months earlier she had tried to procure an abortion by drinking an infusion of wormwood leaves, but that to their knowledge had not tried since. On Examination she was an obese woman, quite conscious although complaining of headache; not dehydrated, BP 130/75 mm. Hg. and with a left upper motor neurone facial paralysis. She was given phenobarbitone 200 mg. i.m. A few hours later she had another grand mal fit from which she never regained consciousness. She continued to have twitch- ing movements of the left face, especially the angle of the mouth and left arm lasting for five minutes and stopping for about the same period before resuming. Increased doses of phenobarbitone and paraldehyde were given to no avail and so a continuous infusion of Brietal (Methohexitone sodium) was set up and her fits became controllable. On the 2nd May a complete abortion took place. A lumbar puncture done on 30.4.64 showed a protein of 60 mg./100 ml. but on 5.5.64 it was 30 mg. The pressure was over 300 mm. 'On the 4th May, 1964, it was noticed that the face and scalp were swollen with engorgement of the temporal veins. The breathing was now being maintained with difficulty due to the quantity of Brietal required to stop the fits. In consequence a tracheostomy was performed and continuous ventila- tion maintained with a ventilator. On 6.5.64 she had a right carotid angiogram performed and this showed no filling of the superior sagittal sinus, with enlargement of draining venous sinuses. See Fig. 1. * Now Medical Adviser to John Wyeth & Co., Hintercombe Lane, Taplow, Nr. Slough, Bucks. She showed no improvement and died on the 8th May, 1964. Necropsy revealed body of obese young woman with a tracheostomy wound. There was marked pul- monary oedema and areas of lung collapse especially in the right lower lobe. Pericardium showed excess fluid. The uterus was moderately enlarged and soft containing dark coloured retained products. No pulmonary infarcts were seen. The Head (A. L. Wolff).-The superior sagittal sinus contained dark maroon coloured antemortem thrombus highly adherent to the walls of the sinus and extending for its whole length. The posterior one-third was paler and older, not completely block- ing the opening of the straight sinus which was free of thrombus, but extending into the left transverse sinus and thence to the left jugular vein for 2 cm. into the neck. The cortical veins on both hemispheres contained antemortem clot with discolouration of precentral convolution on right side due to haemor- rhagic infarction. Dissection after fixation showed white thrombus in left and right Rolandic veins and superior cerebral veins running in the inferior frontal sulcus. The middle frontal convolution dorsal to this vein was soft with haemorrhage. Coronal section showed two small haematomas, the largest 0.6 cm. x 1.5 cm. on either side of right inferior frontal sulcus. The superior longitudinal sinus was filled with reddish clot except the posterior part where it was whitish-yellow. Here there was evidence of opening of new channels. Histology revealed in the posterior superior longi- tudinal sinus, laminated thrombus, the peripheral parts of which were in an advanced state of organisa- tion with dense fibrous tissue from which fibroblasts were extending into the more recent clot. In some areas there was evidence of digestion of the thrombus by phagocytes. Discussion This case demonstrates well some of the classical clinical features of superior sagittal sinus thrombosis. The onset with a grand mal fit, followed by unilateral convulsions and headache, was first described by Gowers (1888) in children and is due to cortical vein thrombosis. The presence, after a few days, of fullness of the temporal veins and choked optic discs was re- corded by Oppenheimer, 1911. It is often as- sociated with oedema of the scalp, the "oedema en casque" of Elieder, Froideval, and Delherine (1956). There are few recorded cases of spontaneous thrombosis of the superior sagittal sinus in preg- nancy-Bristow, 1888; Biicklers, 1893; Stertz, 1909; Fishman, Cowen and Silberman, 1957. Thickotter (1891) described a case with con- Case Report A CASE OF Protected by copyright. on 13 February 2019 by guest. http://pmj.bmj.com/ Postgrad Med J: first published as 10.1136/pgmj.41.481.702 on 1 November 1965. Downloaded from

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POSTGRAD. MED. J. (1965), 41, 702.

SUPERIOR LONGITUDINAL SINUS THROMBOSISIN PREGNANCY

D. J. RICHARDS, B.Sc., M.B., Ch.B., M.R.C.S.,L.R.C.P.*

Registrar in General Medicine,Hallam Hospital, West Bromwich.

PRIMARY (aseptic, marasmic or autochthonous)thrombosis of the superior sagittal sinus, that iswhere local inflammation plays no part (Bertier,1907), is an uncommon condition.

It was first noted that the puerperium couldpredispose to its formation by Gowers (1888),but description of cases occurring during preg-nancy itself are rare.

Case ReportMrs. B.M., aged 29 years, was admitted on the

29th April, 1964, to Hallam Hospital, West Brom-wich. She was 12 weeks pregnant and had beenvomiting fairly consistently for eight weeks. Thegeneral practitioner had diagnosed this as hyper-emesis gravidarum and had treated her with pro-chlorperazine (Stemetil). On the day of admissionshe was found in bed having a generalised fit withtongue biting and incontinence. There was nohistory of epileptic convulsions in the family. Theprevious three pregnancies in 1956, 58 and 62 wereuneventful apart from a post-partum haemorrhagewith the first.The relatives stated that two months earlier she

had tried to procure an abortion by drinking aninfusion of wormwood leaves, but that to theirknowledge had not tried since.On Examination she was an obese woman, quite

conscious although complaining of headache; notdehydrated, BP 130/75 mm. Hg. and with a leftupper motor neurone facial paralysis. She was givenphenobarbitone 200 mg. i.m. A few hours latershe had another grand mal fit from which she neverregained consciousness. She continued to have twitch-ing movements of the left face, especially the angleof the mouth and left arm lasting for five minutesand stopping for about the same period beforeresuming.

Increased doses of phenobarbitone and paraldehydewere given to no avail and so a continuous infusionof Brietal (Methohexitone sodium) was set up andher fits became controllable. On the 2nd May acomplete abortion took place.A lumbar puncture done on 30.4.64 showed a

protein of 60 mg./100 ml. but on 5.5.64 it was 30 mg.The pressure was over 300 mm.

'On the 4th May, 1964, it was noticed that theface and scalp were swollen with engorgement ofthe temporal veins. The breathing was now beingmaintained with difficulty due to the quantity ofBrietal required to stop the fits. In consequence atracheostomy was performed and continuous ventila-tion maintained with a ventilator. On 6.5.64 shehad a right carotid angiogram performed and thisshowed no filling of the superior sagittal sinus, withenlargement of draining venous sinuses. See Fig. 1.* Now Medical Adviser to John Wyeth & Co.,Hintercombe Lane, Taplow, Nr. Slough, Bucks.

She showed no improvement and died on the 8thMay, 1964.Necropsy revealed body of obese young woman

with a tracheostomy wound. There was marked pul-monary oedema and areas of lung collapse especiallyin the right lower lobe. Pericardium showed excessfluid. The uterus was moderately enlarged and softcontaining dark coloured retained products. Nopulmonary infarcts were seen.The Head (A. L. Wolff).-The superior sagittal

sinus contained dark maroon coloured antemortemthrombus highly adherent to the walls of the sinusand extending for its whole length. The posteriorone-third was paler and older, not completely block-ing the opening of the straight sinus which was freeof thrombus, but extending into the left transversesinus and thence to the left jugular vein for 2 cm.into the neck. The cortical veins on both hemispherescontained antemortem clot with discolouration ofprecentral convolution on right side due to haemor-rhagic infarction.

Dissection after fixation showed white thrombus inleft and right Rolandic veins and superior cerebralveins running in the inferior frontal sulcus. Themiddle frontal convolution dorsal to this vein wassoft with haemorrhage.Coronal section showed two small haematomas, the

largest 0.6 cm. x 1.5 cm. on either side of rightinferior frontal sulcus. The superior longitudinalsinus was filled with reddish clot except the posteriorpart where it was whitish-yellow. Here there wasevidence of opening of new channels.

Histology revealed in the posterior superior longi-tudinal sinus, laminated thrombus, the peripheralparts of which were in an advanced state of organisa-tion with dense fibrous tissue from which fibroblastswere extending into the more recent clot. In someareas there was evidence of digestion of the thrombusby phagocytes.

DiscussionThis case demonstrates well some of the

classical clinical features of superior sagittal sinusthrombosis. The onset with a grand mal fit,followed by unilateral convulsions and headache,was first described by Gowers (1888) in childrenand is due to cortical vein thrombosis. Thepresence, after a few days, of fullness of thetemporal veins and choked optic discs was re-corded by Oppenheimer, 1911. It is often as-sociated with oedema of the scalp, the "oedemaen casque" of Elieder, Froideval, and Delherine(1956).There are few recorded cases of spontaneous

thrombosis of the superior sagittal sinus in preg-nancy-Bristow, 1888; Biicklers, 1893; Stertz,1909; Fishman, Cowen and Silberman, 1957.Thickotter (1891) described a case with con-

Case Report

A CASE OF

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FIG. 2.-Antemortem clot present in superior sagittalsinus and the cortical veins together withhaemorrhagic infarction of the right precentralconvolution.

vulsions and loss of consciousness in the firstpregnancy recurring in the second pregnancy.The patient died in the puerperium with throm-bosis of the left transverse sinus, straight sinus andvein of Galen. Prokess (1900) had a case ofsuperior sagittal sinus thrombosis of unknownaetiology where the patient was moribund, buta living child was delivered by Caesarian Section.In Duggelin's case (1939), the symptoms began

in the second half of pregnancy even though thediagnosis was made in the puerperium. Extensivethrombosis of the cerebral veins but not of thesuperior sagittal sinus was noted by Hensell (1961)in the first month of pregnancy.The macroscopic and microscopic appearances

of the posterior one-third of the clot in thesuperior sagittal sinus suggested that it had beenpresent for some time, certainly months beforethe onset of the terminal illness, and could pos-sibly have occurred in a previous pregnancy asin Thickotter's case.

I wish to thank Dr. J. V. S. A. Davies for per-mission to publish this case, to Dr. A. L. Wolff forgreat help in pathological data and to Mr. Gassenfor the photography.

REFERENCESBERTIER, J. '(1907): La Thrombose Medicale des Sinus

de la Dure-mere., Arch., Gen. de Med., 1, 313.BRISTOWE, J. S. (1894): On Intracranial Surgery-

Edinb. Med. J., 39, 1084.BUCKLERS, J. (1893): Zwei Falle von Autochthoner

Hirnsinus Thrombose, Arch. Psychiat. Nervenkr.,25, 18.

DUGGELIN, M. (1939): Ueber die primare SinusThrombose in Wockenbett, Inag. Diss. Zurich.

ELIEDER, E., FROIDEVAL, G., and DELHERINE, A.(1956): Thrombophlebite du Sinus LongitudinalSuperieur d'origine Sinusieene, Arch. franc Pediat.,13, 760.

FISHMAN, R. A., COWEN, M. D., and SILBERMAN, M.(1957): Neurology (Minneap.), 7, 217.

GOWERS, W. (1888): A Manual of Diseases of theNervous System, Vol. 2, 416, London: Churchill.

HENSELL, V. (1961): Traumatische Hirnsinus andVenenthrombosen, Acta. Psychiat. Scand., 38, 730.

OPPENHEIMER, H. (1911): Textbook of NervousDiseases for Physicians and Students, 5th Edition,Edinburgh: Schultze.

PROKESS, A. (1900): Sectio Caesarea in Moribunda,Zbl. Gynak., p. 214.

STERTZ, G. (1909): Katatonische Psychose als Sympto-metisches Bild bei Sinus Thrombose, Berl. klin.Wschr., 46, 685.

THICKTrrER, J. (1891): Ueber einem Fall von maran-tischer Sinus Thrombose in Puerperium, Inaug. Diss.Munich.

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ovember 1965. D

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